Integra LifeSciences Holdings Corporation (NASDAQ: IART) today
reported financial results for the fourth quarter and full year
ended December 31, 2024.
Fourth Quarter 2024
- Reported revenues were $442.6 million, representing an increase
of 11.5% on a reported basis and an increase of 3.5% on an organic
basis compared to the fourth quarter 2023.
- GAAP earnings per diluted share were $0.25, compared to $0.25
in the fourth quarter 2023.
- Adjusted earnings per diluted share were $0.97, compared to
$0.89 in the fourth quarter 2023.
Full-Year 2024
- Reported revenues were $1,610.5 million, representing an
increase of 4.5% on a reported basis and a decrease of 1.3% on an
organic basis compared to full-year 2023.
- GAAP earnings per diluted share were $(0.09), compared to $0.84
in 2023.
- Adjusted earnings per diluted share were $2.56, compared to
$3.10 in 2023.
2024 Business Highlights
- Appointed Mojdeh Poul as President & CEO
- Experienced strong demand for our differentiated portfolio of
leading brands
- Initiated the Compliance Master Plan, an enterprise-wide
approach to enhance quality management systems
- Made critical investments in capacity and supply
reliability
- Integrated the Acclarent acquisition successfully
- Realized strong market uptake of CereLink®
- Announced transition of manufacturing of PriMatrix® and
SurgiMend® to Braintree, Massachusetts in the first half of
2026
- Advanced PMA submission for DuraSorb® and received PMA
approvable notification pending GMP certification for
SurgiMend
- Expanded international commercial footprint and portfolio;
advanced in-China-for-China manufacturing build-out
"As I step into my role leading Integra, I am
inspired by the strength of our portfolio, the dedication of our
team, and the tremendous potential we have to grow and innovate in
high-impact specialty markets. Our fourth-quarter results reflect
this strength, with sequential revenue growth driven by robust
demand for our leading brands, continued progress in expanding our
global presence, and our ongoing commitment to improving supply
reliability," said Mojdeh Poul, president and chief executive
officer.
"While there is significant work ahead to enhance
our quality system and streamline our processes, I am confident in
our ability to address these challenges and position Integra for
long-term, sustainable growth. By leveraging our competitive
strengths, differentiated technologies, commercial expertise, and
global presence, we are poised to unlock new opportunities for
innovation and deliver greater value to our customers, patients,
and shareholders."
Fourth Quarter 2024 Financial
Summary
Total reported revenues for the fourth quarter
were $442.6 million, an increase of 11.5% from the fourth quarter
of 2023. Fourth quarter organic revenues were up 3.5% compared to
the prior year.
The Company reported GAAP net income of $19.4
million, or $0.25 per diluted share, in the fourth quarter of 2024,
compared to GAAP net income of $19.8 million, or $0.25 per diluted
share, in the prior year.
Adjusted EBITDA for the fourth quarter of 2024 was
$104.9 million, compared to $100.5 million in the fourth quarter of
2023. As a percentage of revenue, adjusted EBITDA was 23.7%, a
decrease of 160 basis points from the prior year period.
Adjusted net income for the fourth quarter of 2024
was $73.3 million, or $0.97 per diluted share, compared to adjusted
net income of $69.1 million, or $0.89 per diluted share, in the
fourth quarter of 2023.
Cash flows from operations totaled $50.7 million
in the fourth quarter and capital expenditures were $29.6
million.
Fourth Quarter 2024 Segment Performance
- Codman Specialty Surgical (71% of Revenues)
- Total revenues were $314.7 million, representing reported an
increase of 15.8% and 4.1% on an organic basis compared to the
fourth quarter of 2023.
- Sales in Neurosurgery grew 5.1% on an organic basis:
- CSF management grew low double-digits driven by BactiSeal® and
Certas® Plus
- Neuro monitoring grew high single-digits driven by CereLink ICP
monitors, BactiSeal and CerebroFlo® EVD catheters.
- Advanced energy grew low single-digits driven by CUSA®
disposables
- Dural access and repair declined low single-digits due to the
impact from the recall of patties and strips partially offset by
growth in DuraGen®, DuraSeal® and Mayfeild®.
- Sales of Instruments were flat on an organic basis due to
growth in hospital sales offset by a decrease in alternative site
sales due to order timing.
- ENT reported revenue growth driven primarily by the Acclarent
acquisition.
- Tissue Technologies (29% of Revenue)
- Total revenues were $128.0 million, representing an increase of
2.1% on a reported and organic basis compared to the fourth quarter
of 2023.
- Sales in Wound Reconstruction grew 8.2% on an organic basis:
- Low-double-digit growth in DuraSorb®, MicroMatrix®, Cytal® and
AmnioExcel®
- Mid-single-digit growth in Integra Skin
- Sales in private label were down 16% on an organic basis due to
a component supply delay
Full-Year 2024 Financial
Summary
Total reported revenues for the full-year 2024
were $1,610.5 million, an increase of 4.5%, from the prior year.
Organic sales for the full-year 2024 were down 1.3% compared to
2023. 2024 Revenues were driven by three quarters of revenue from
the Acclarent acquisition offset by production constraints on
Integra Skin and intermittent ship holds on various products.
The Company reported GAAP net income of $(6.9)
million, or $(0.09) per diluted share, for the full-year 2024,
compared to GAAP net income of $67.7 million, or $0.84 per diluted
share in 2023.
Adjusted EBITDA for the full-year 2024 was $322.2
million, a decrease of $47.4 million versus the prior year. Full-
year adjusted EBITDA margins were 20.0%, a decrease of 400 basis
points from the prior year.
Adjusted net income for the full-year 2024 was
$196.9 million, or $2.56 per diluted share, compared to $247.8
million, or $3.10 per diluted share in the prior year.
2024 Balance Sheet, Cash Flow and Capital
Allocation
The Company generated cash flow from operations of
$129.4 million for the full-year 2024. Full-year capital
expenditures were $104.0 million. Net debt at the end of the year
was $1.5 billion, and the consolidated total leverage ratio was
4.0x. As of year-end, the Company had total liquidity of
approximately $1.2 billion, including approximately $273 million in
cash plus short-term investments and the remainder available under
its revolving credit facility.
2025 Revenue and Adjusted Earnings Per
Share Guidance
For the full-year 2025, the Company expects
revenues to be in the range of $1,650 million to $1,715 million,
representing reported growth of 2.4% to 6.5% and organic growth of
1.0% to 5.0%. 2025 revenue guidance reflects the strong demand for
the Company’s portfolio and a full year of the Acclarent
acquisition offset by the potential for intermittent ship holds as
the company continues to implement its Compliance Master Plan and
the strength of the U.S. dollar. Adjusted earnings per diluted
share are expected to be between $2.41 and $2.51.
For the first quarter 2025, the Company expects
reported revenues in the range of $375 million to $385 million,
representing reported growth of 1.6% to 4.4% and organic growth of
-6.2% to -3.5%. First quarter 2025 revenue guidance reflects the
benefit of the Acclarent acquisition offset by temporary production
delays on Integra Skin, intermittent ship-holds as the company
continues to implement its Compliance Master Plan and the strength
of the U.S. dollar. Adjusted earnings per diluted share are
expected to be in the range of $0.40 to $0.45.
Organic sales growth excludes acquisitions as well
as the effects of foreign currency.
The Company is providing forward-looking guidance
regarding adjusted earnings per diluted share but is not providing
a reconciliation to GAAP earnings per share, because certain GAAP
expense items are highly variable, and management is unable to
predict them with reasonable certainty and without unreasonable
effort. Specifically, the financial impact and timing of
divestitures, acquisitions, integrations, structural optimization
and efforts to comply with the EU Medical Device Regulation are
uncertain, depend on various dynamic factors and are not reasonably
ascertainable at this time. These expense items could have a
material impact on GAAP results.
Conference Call and Presentation Available
Online
Integra has scheduled a conference call for 8:30
a.m. ET on Tuesday, February 25, 2025, to discuss fourth quarter
and full-year 2024 financial results, and forward-looking financial
guidance. The conference call will be hosted by Integra's senior
management team and will be open to all listeners. Additional
forward-looking information may be discussed in a
question-and-answer session following the call. Integra's
management team will reference a presentation during the conference
call, which can be found on the Investor Relations section of the
website at investor.integralife.com.
A live webcast will be available on the Investors
section of the Company’s website at investor.integralife.com. For
those planning to participate on the call, please register here to
receive dial-in details and a unique pin. While not required, it is
recommended to join 10 minutes prior to the start of the event. A
webcast replay of the conference call will be available on the
Investor Relations section of the Company’s website following the
call.
About Integra At Integra
LifeSciences, we are driven by our purpose of restoring patients’
lives. We innovate treatment pathways to advance patient outcomes
and set new standards of surgical, neurologic, and regenerative
care. We offer a comprehensive portfolio of high quality,
leadership brands. For the latest news and information about
Integra and its products, please visit www.integralife.com.
Forward-Looking Statements
This news release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995 that involve risks and uncertainties and reflect
the Company's judgment as of the date of this release. All
statements, other than statements of historical fact, are
statements that could be deemed forward-looking statements. Some of
these forward-looking statements may contain words like “will,”
“believe,” “may,” “could,” “would,” “might,” “possible,” “should,”
“expect,” “intend,” "forecast," "guidance," “plan,” “anticipate,”
"target," or “continue,” the negative of these words, other terms
of similar meaning or they may use future dates. Forward-looking
statements contained in this news release include, but are not
limited to, statements concerning future financial performance,
including projections for revenues, expected revenue growth (both
reported and organic), GAAP and adjusted net income, GAAP and
adjusted earnings per diluted share, non-GAAP adjustments such as
divestiture, acquisition and integration-related charges,
intangible asset amortization, structural optimization charges, EU
Medical Device Regulation-related charges, charges related to the
voluntary global recall of all products manufactured at the
Company’s facility in Boston, Massachusetts and the transition of
Boston-related manufacturing operations to the Company’s Braintree,
Massachusetts facility, and income tax expense (benefit) related to
non-GAAP adjustments and other items, and the Company’s
expectations and plans with respect to business and operational
performance, strategic initiatives, capabilities, resources,
product development, product availability and regulatory approvals,
including expectations regarding the efficacy of the Company’s
compliance master plan to improve the Company's quality system. It
is important to note that the Company’s goals and expectations are
not predictions of actual performance. Such forward-looking
statements involve risks and uncertainties that could cause actual
results to differ materially from predicted or expected results.
Such risks and uncertainties include, but are not limited, to the
following: the ongoing and possible future effects of global
challenges, including macroeconomic uncertainties, inflation,
supply chain disruptions, trade regulation and tariffs, bank
failures and other economic disruptions, and U.S. and global
recession concerns, on the Company’s customers and on the Company’s
business, financial condition, results of operations and cash
flows; the Company's ability to execute its operating plan
effectively; the Company’s ability to successfully integrate
Acclarent and other acquired businesses; the Company’s ability to
achieve sales growth in a timely fashion; the Company's ability to
manufacture and ship sufficient quantities of its products to meet
its customers' demands; the ability of third-party suppliers to
supply us with raw materials and finished products; global
macroeconomic and political conditions, including the war in
Ukraine and the conflict in Israel and Gaza; the Company's ability
to manage its direct sales channels effectively; the sales
performance of third-party distributors on whom the Company relies
to generate revenue for certain products and geographic regions;
the Company's ability to access and maintain relationships with
customers of acquired entities and businesses; physicians'
willingness to adopt and third-party payors' willingness to provide
or maintain reimbursement for the Company's recently launched,
planned and existing products; initiatives launched by the
Company's competitors; downward pricing pressures from customers;
the Company's ability to secure regulatory approval for products in
development; the Company's ability to remediate quality systems
violations; difficulties in implementing the Company’s compliance
master plan and realizing the benefits contemplated thereby within
the anticipated timeframe, or at all; difficulties or delays in
obtaining and maintaining required regulatory approvals related to
the transition of the manufacturing to the Company’s Braintree
manufacturing facility; the possibility that costs or difficulties
related to building and the operationalization of the Braintree
facility or the transition of manufacturing activities from the
Company’s Boston facility to the Braintree facility will be greater
than expected; fluctuations in hospitals' spending for capital
equipment; uncertainties inherent in the development of new
products and the enhancement of existing products, including FDA
approval and/or clearance and other regulatory risks, technical
risks, cost overruns and delays; the Company's ability to comply
with regulations regarding products of human origin and products
containing materials derived from animal source; difficulties in
controlling expenses, including costs to procure and manufacture
the Company’s products; the ability of the Company to successfully
manage leadership and organizational changes and the impact of
changes in management or staff levels; the impact of goodwill and
intangible asset impairment charges if future operating results of
acquired businesses are significantly less than the results
anticipated at the time of the acquisitions, the Company's ability
to leverage its existing selling organizations and administrative
infrastructure; the Company's ability to increase product sales and
gross margins, and control non-product costs; the Company’s ability
to achieve anticipated growth rates, margins and scale and execute
its strategy generally; the amount and timing of divestiture,
acquisition and integration-related costs; the geographic
distribution of where the Company generates its taxable income; new
U.S. and foreign government laws and regulations, and changes in
existing laws, regulations and enforcement guidance, which affect
areas of our operations including, but not limited to, those
affecting the health care industry, including the EU Medical Device
Regulation; the scope, duration and effect of U.S. and
international governmental, regulatory, fiscal, monetary and public
health responses to any future public health crises; fluctuations
in foreign currency exchange rates; the amount of our bank
borrowings outstanding and other factors influencing liquidity;
potential negative impacts resulting from environmental, social and
governance matters; and the economic, competitive, governmental,
technological, and other risk factors and uncertainties identified
under the heading “Risk Factors” included in Item 1A of Integra's
Annual Report on Form 10-K for the year ended December 31, 2024 to
be filed with the Securities and Exchange Commission.
These forward-looking statements are made only as
of the date hereof, and the Company undertakes no obligation to
update or revise the forward-looking statements, whether as a
result of new information, future events, or otherwise, except as
required by law.
Discussion of Adjusted Financial Measures
In addition to our GAAP results, we provide
certain non-GAAP measures, including organic revenues, adjusted
earnings before interest, taxes, depreciation and amortization
("EBITDA"), adjusted EBITDA margin, adjusted net income, adjusted
gross profit, adjusted gross margin, adjusted earnings per diluted
share, free cash flow, adjusted free cash flow conversion, and net
debt. Organic revenues consist of total revenues excluding the
effects of currency exchange rates, revenues from current-period
acquisitions and product divestitures. Adjusted EBITDA consists of
GAAP net income excluding: (i) depreciation and amortization; (ii)
other income (expense); (iii) interest income and expense; (iv)
income tax expense (benefit); and (v) those operating expenses also
excluded from adjusted net income. The measure of adjusted EBITDA
margin is calculated by dividing adjusted EBITDA by total revenues.
The measure of adjusted net income consists of GAAP net income,
excluding: (i) structural optimization charges; (ii) divestiture,
acquisition and integration-related charges; (iii) EU Medical
Device Regulation-related charges; (iv) charges related to the
voluntary global recall of products manufactured at the Company’s
Boston, Massachusetts facility and distributed between March 1,
2018 and May 22, 2023, as previously disclosed in the Company’s
Current Report on Form 8-K filed with the Securities and Exchange
Commission on May 23, 2023 (the “recall”) and the transition of
Boston-related manufacturing operations to the Company’s Braintree,
Massachusetts facility; (v) intangible asset amortization expense;
and (vi) income tax impact from adjustments. The measure of
adjusted gross margin is calculated by dividing adjusted gross
profit by total revenues. Adjusted gross profit consists of GAAP
gross profit adjusted for: (i) structural optimization charges;
(ii) divestiture, acquisition and integration-related charges;
(iii) charges related to the recall and the transition of
Boston-related manufacturing operations to the Company’s Braintree,
Massachusetts facility; (iv) EU Medical Device Regulation-related
charges; and (v) intangible asset amortization expense. The
adjusted earnings per diluted share measure is calculated by
dividing adjusted net income attributable to diluted shares by
diluted weighted average shares outstanding. The measure of free
cash flow consists of GAAP net cash provided by operating
activities less purchases of property and equipment. The adjusted
free cash flow conversion measure is calculated by dividing free
cash flow by adjusted net income. The measure of net debt consists
of GAAP total debt (excluding deferred financing costs) less
short-term investments, cash and cash equivalents.
Reconciliations of GAAP revenues to organic
revenues, GAAP net income to adjusted EBITDA and adjusted net
income, GAAP gross profit to adjusted gross profit, GAAP gross
margin to adjusted gross margin, and GAAP earnings per diluted
share to adjusted earnings per diluted share all for the quarters
and years ended December 31, 2024 and 2023, GAAP total debt to net
debt for the years ended December 31, 2024 and 2024, and the GAAP
operating cash flow to free cash flow and adjusted free cash flow
conversion for the quarters and years ended December 31, 2024 and
2023, appear in the financial tables in this release.
The Company believes that the presentation of
organic revenues and the other non-GAAP measures provide important
supplemental information to management and investors regarding
financial and business trends relating to the Company's financial
condition and results of operations. For further information
regarding why Integra believes that these non-GAAP financial
measures provide useful information to investors, the specific
manner in which management uses these measures, and some of the
limitations associated with the use of these measures, please refer
to the Company's Current Report on Form 8-K regarding this earnings
press release filed today with the Securities and Exchange
Commission. This Current Report on Form 8-K is available on the
SEC's website at www.sec.gov or on our website at
www.integralife.com.
Investor Relations
Contact:
Chris Ward (609) 772-7736
chris.ward@integralife.com
Media Contact:
Laurene Isip (609) 208-8121
laurene.isip@integralife.com
|
|
|
|
INTEGRA LIFESCIENCES HOLDINGS CORPORATIONCONDENSED CONSOLIDATED
STATEMENTS OF OPERATIONS(UNAUDITED) |
|
|
|
|
(In thousands, except per
share amounts) |
|
|
|
|
|
|
|
|
Three Months Ended December 31, |
|
Twelve Months Ended December 31, |
|
2024 |
|
2023 |
|
2024 |
|
2023 |
Total revenues |
442,645 |
|
|
397,039 |
|
|
1,610,527 |
|
|
1,541,573 |
|
|
|
|
|
|
|
|
|
Costs and expenses: |
|
|
|
|
|
|
|
Cost of goods sold |
193,573 |
|
|
170,546 |
|
|
728,466 |
|
|
656,838 |
|
Research and development |
31,210 |
|
|
24,284 |
|
|
115,377 |
|
|
104,192 |
|
Selling, general and administrative |
178,520 |
|
|
163,128 |
|
|
716,983 |
|
|
656,641 |
|
Intangible asset amortization |
3,715 |
|
|
3,034 |
|
|
21,290 |
|
|
12,376 |
|
Total costs and expenses |
407,018 |
|
|
360,992 |
|
|
1,582,116 |
|
|
1,430,047 |
|
Operating income |
35,627 |
|
|
36,047 |
|
|
28,411 |
|
|
111,526 |
|
Interest income |
4,893 |
|
|
4,549 |
|
|
20,040 |
|
|
17,202 |
|
Interest expense |
(18,984 |
) |
|
(13,751 |
) |
|
(70,632 |
) |
|
(51,377 |
) |
Gain (loss) from the sale of business |
— |
|
|
— |
|
|
— |
|
|
— |
|
Other income, net |
1,005 |
|
|
2,013 |
|
|
3,944 |
|
|
3,718 |
|
Income (loss) before taxes |
22,541 |
|
|
28,858 |
|
|
(18,237 |
) |
|
81,069 |
|
Income tax expense (benefit) |
3,106 |
|
|
9,024 |
|
|
(11,293 |
) |
|
13,328 |
|
Net income (loss) |
19,435 |
|
|
19,834 |
|
|
(6,944 |
) |
|
67,741 |
|
|
|
|
|
|
|
|
|
Net income (loss) per share: |
|
|
|
|
|
|
|
Diluted net income (loss) per share |
0.25 |
|
|
0.25 |
|
|
(0.09 |
) |
|
0.84 |
|
Weighted average common shares outstanding for diluted net income
per share |
76,419 |
|
|
77,959 |
|
|
77,010 |
|
|
80,337 |
|
|
|
|
|
|
|
|
|
Segment revenues and growth in total revenues
excluding the effects of currency exchange rates, acquisitions and
discontinued products are as follows:
(In thousands)
|
Three Months Ended December 31, |
|
Twelve Months Ended December 31, |
|
2024 |
2023 |
Change |
|
2024 |
2023 |
Change |
Neurosurgery |
220,091 |
|
210,204 |
|
4.7 |
% |
|
803,816 |
|
818,101 |
|
(1.7 |
)% |
Instruments |
51,029 |
|
51,095 |
|
(0.1 |
)% |
|
204,177 |
|
203,617 |
|
0.3 |
% |
ENT |
43,540 |
|
10,328 |
|
321.6 |
% |
|
135,643 |
|
37,275 |
|
263.9 |
% |
Total Codman Specialty Surgical |
314,660 |
|
271,627 |
|
15.8 |
% |
|
1,143,636 |
|
1,058,993 |
|
8.0 |
% |
|
|
|
|
|
|
|
|
|
Wound Reconstruction and Care |
101,527 |
|
93,859 |
|
8.2 |
% |
|
350,565 |
|
373,986 |
|
(6.3 |
)% |
Private Label |
26,458 |
|
31,553 |
|
(16.1 |
)% |
|
116,326 |
|
108,594 |
|
7.1 |
% |
Total Tissue Technologies |
127,985 |
|
125,412 |
|
2.1 |
% |
|
466,891 |
|
482,580 |
|
(3.3 |
)% |
Total Reported Revenues |
442,645 |
|
397,039 |
|
11.5 |
% |
|
1,610,527 |
|
1,541,573 |
|
4.5 |
% |
|
|
|
|
|
|
|
|
|
Impact of changes in currency exchange rates |
880 |
|
— |
|
— |
|
|
6,084 |
|
— |
|
— |
|
Less contribution of revenues from acquisitions |
(32,763 |
) |
— |
|
— |
|
|
(95,049 |
) |
— |
|
— |
|
Less contribution of revenues from divested products |
— |
|
— |
|
— |
|
|
— |
|
(245 |
) |
— |
|
Less contribution of revenues from discontinued products |
— |
|
— |
|
— |
|
|
— |
|
— |
|
— |
|
Total organic revenues1 |
410,762 |
|
397,039 |
|
3.5 |
% |
|
1,521,563 |
|
1,541,328 |
|
(1.3 |
)% |
|
|
|
|
|
|
|
|
|
(1) Organic revenues have been adjusted to exclude
foreign currency (current period), acquisitions and to account for
divested and discontinued products.
Items included in GAAP net income and from
continuing operations and locations where each item is recorded are
as follows:
(In thousands)
Three Months Ended December 31, 2024 |
|
|
|
|
|
|
|
|
|
|
|
|
|
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort.(d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
2,264 |
|
513 |
|
315 |
|
1,034 |
|
— |
|
402 |
|
— |
|
Structural Optimization charges |
9,083 |
|
4,238 |
|
4,261 |
|
583 |
|
— |
|
— |
|
— |
|
EU Medical Device Regulation charges |
9,461 |
|
1,054 |
|
3,933 |
|
4,474 |
|
— |
|
— |
|
— |
|
Boston Recall/Braintree Transition |
11,358 |
|
10,966 |
|
392 |
|
— |
|
— |
|
— |
|
— |
|
Intangible asset amortization expense |
26,557 |
|
22,842 |
|
— |
|
— |
|
3,715 |
|
— |
|
— |
|
Estimated income tax impact from above adjustments and other
items |
(4,902 |
) |
— |
|
— |
|
— |
|
— |
|
— |
|
(4,902 |
) |
Depreciation expense |
10,935 |
|
— |
|
— |
|
— |
|
— |
|
— |
|
— |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
a) |
COGS - Cost of
goods sold |
|
b) |
SG&A - Selling, general and administrative |
|
c) |
R&D - Research & development |
|
d) |
Amort. - Intangible asset amortization |
|
e) |
OI&E - Other income & expense |
|
f) |
Tax - Income tax expense (benefit) |
|
|
|
Three Months Ended December 31, 2023 |
|
|
|
|
|
|
|
|
|
|
|
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort.(d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
7,117 |
|
73 |
|
8,040 |
|
(880 |
) |
— |
|
(116 |
) |
— |
|
Structural Optimization charges |
6,216 |
|
3,077 |
|
3,155 |
|
(16 |
) |
— |
|
— |
|
— |
|
EU Medical Device Regulation charges |
12,387 |
|
2,227 |
|
4,653 |
|
5,507 |
|
— |
|
— |
|
— |
|
Boston Recall/Braintree Transition |
8,129 |
|
7,370 |
|
759 |
|
— |
|
— |
|
— |
|
— |
|
Intangible asset amortization expense |
20,687 |
|
17,653 |
|
— |
|
— |
|
3,034 |
|
— |
|
— |
|
Estimated income tax impact from above adjustments and other
items |
(5,272 |
) |
— |
|
— |
|
— |
|
— |
|
— |
|
(5,272 |
) |
Depreciation expense |
9,834 |
|
— |
|
— |
|
— |
|
— |
|
— |
|
— |
|
|
|
|
|
|
|
|
|
|
|
|
|
(a) |
COGS - Cost of
goods sold |
|
(b) |
SG&A - Selling, general and administrative |
|
(c) |
R&D - Research & development |
|
(d) |
Amort. - Intangible asset amortization |
|
(e) |
OI&E - Other income & expense |
|
(f) |
Tax - Income tax expense (benefit) |
|
|
|
Items included in GAAP net income and location
where each item is recorded are as follows:
(In thousands)
Twelve Months Ended December 31, 2024 |
|
|
|
|
|
|
|
|
|
|
|
|
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort.(d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
33,626 |
|
9,071 |
|
25,793 |
|
(1,542 |
) |
— |
|
304 |
|
— |
|
Structural Optimization charges |
24,194 |
|
16,195 |
|
7,395 |
|
604 |
|
— |
|
— |
|
— |
|
EU Medical Device Regulation charges |
44,570 |
|
4,020 |
|
18,875 |
|
21,674 |
|
— |
|
— |
|
— |
|
Boston Recall |
45,034 |
|
43,175 |
|
1,859 |
|
— |
|
— |
|
— |
|
— |
|
Intangible asset amortization expense |
105,252 |
|
83,962 |
|
— |
|
— |
|
21,290 |
|
— |
|
— |
|
Estimated income tax impact from above adjustments and other
items |
(48,792 |
) |
— |
|
— |
|
— |
|
— |
|
— |
|
(48,792 |
) |
Depreciation expense |
41,449 |
|
— |
|
— |
|
— |
|
— |
|
— |
|
— |
|
|
(a) |
COGS - Cost of
goods sold |
|
(b) |
SG&A - Selling, general and administrative |
|
(c) |
R&D - Research & development |
|
(d) |
Amort. - Intangible asset amortization |
|
(e) |
OI&E - Other income & expense |
|
(f) |
Tax - Income tax expense (benefit) |
|
|
|
Twelve Months Ended December 31, 2023 |
|
|
|
|
|
|
|
|
|
|
|
Item |
Total Amount |
COGS(a) |
SG&A(b) |
R&D(c) |
Amort.(d) |
OI&E(e) |
Tax(f) |
Acquisition, divestiture and integration-related charges |
25,173 |
|
3,045 |
|
25,181 |
|
(2,188 |
) |
— |
|
(865 |
) |
— |
|
Structural Optimization charges |
16,084 |
|
8,208 |
|
7,943 |
|
(67 |
) |
— |
|
— |
|
— |
|
EU Medical Device Regulation charges |
46,559 |
|
5,813 |
|
20,002 |
|
20,745 |
|
— |
|
— |
|
— |
|
Boston Recall |
46,970 |
|
46,116 |
|
853 |
|
— |
|
— |
|
— |
|
— |
|
Intangible asset amortization expense |
82,823 |
|
70,447 |
|
— |
|
— |
|
12,376 |
|
— |
|
— |
|
Estimated income tax impact from above adjustments and other
items |
(37,573 |
) |
— |
|
— |
|
— |
|
— |
|
— |
|
(37,573 |
) |
Depreciation expense |
39,704 |
|
— |
|
— |
|
— |
|
— |
|
— |
|
— |
|
|
(a) |
COGS - Cost of
goods sold |
|
(b) |
SG&A - Selling, general and administrative |
|
(c) |
R&D - Research & development |
|
(d) |
Amort. - Intangible asset amortization |
|
(e) |
OI&E - Other income & expense |
|
(f) |
Tax - Income tax expense (benefit) |
|
|
|
INTEGRA LIFESCIENCES HOLDINGS CORPORATION RECONCILIATION OF
NON-GAAP ADJUSTMENTS - GAAP NET INCOME FROM CONTINUING OPERATIONS
TO ADJUSTED EBITDA (UNAUDITED) |
|
|
|
|
(In thousands) |
|
|
|
|
|
|
|
|
Three Months Ended December 31, |
|
Twelve Months Ended December 31, |
|
2024 |
|
2023 |
|
2024 |
|
2023 |
|
|
|
|
|
|
|
|
GAAP net income |
19,435 |
|
|
19,834 |
|
|
(6,944 |
) |
|
67,741 |
|
Non-GAAP adjustments: |
|
|
|
|
|
|
|
Depreciation and intangible asset amortization expense |
37,491 |
|
|
30,522 |
|
|
146,701 |
|
|
122,528 |
|
Other (income), net |
(1,407 |
) |
|
(1,897 |
) |
|
(4,248 |
) |
|
(2,853 |
) |
Interest expense, net |
14,091 |
|
|
9,202 |
|
|
50,591 |
|
|
34,175 |
|
Income tax expense (benefit) |
3,106 |
|
|
9,024 |
|
|
(11,293 |
) |
|
13,328 |
|
Structural optimization charges |
9,083 |
|
|
6,216 |
|
|
24,194 |
|
|
16,084 |
|
EU Medical Device Regulation charges |
9,461 |
|
|
12,387 |
|
|
44,570 |
|
|
46,559 |
|
Boston Recall |
11,358 |
|
|
8,129 |
|
|
45,034 |
|
|
46,970 |
|
Acquisition, divestiture and integration-related charges |
2,264 |
|
|
7,117 |
|
|
33,626 |
|
|
25,173 |
|
Total of non-GAAP adjustments |
85,447 |
|
|
80,700 |
|
|
329,175 |
|
|
301,964 |
|
Adjusted EBITDA |
104,882 |
|
|
100,534 |
|
|
322,231 |
|
|
369,705 |
|
|
|
|
|
|
|
|
|
|
|
|
|
INTEGRA LIFESCIENCES HOLDINGS CORPORATION RECONCILIATION OF
NON-GAAP ADJUSTMENTS - GAAP NET INCOME FROM CONTINUING OPERATIONS
TO MEASURES OF ADJUSTED NET INCOME AND ADJUSTED EARNINGS PER SHARE
(UNAUDITED) |
|
|
|
|
(In thousands, except per share amounts) |
|
|
|
|
|
|
|
|
Three Months Ended December 31, |
|
Twelve Months Ended December 31, |
|
2024 |
|
2023 |
|
2024 |
|
2023 |
|
|
|
|
|
|
|
|
GAAP net income |
|
19,435 |
|
|
19,834 |
|
|
|
(6,944 |
) |
|
67,741 |
|
Non-GAAP adjustments: |
|
|
|
|
|
|
|
Structural optimization charges |
|
9,083 |
|
|
6,216 |
|
|
|
24,194 |
|
|
16,084 |
|
Acquisition, divestiture and integration-related charges |
|
2,264 |
|
|
7,117 |
|
|
|
33,626 |
|
|
25,173 |
|
EU Medical Device Regulation charges |
|
9,461 |
|
|
12,387 |
|
|
|
44,570 |
|
|
46,559 |
|
Boston Recall |
|
11,358 |
|
|
8,129 |
|
|
|
45,034 |
|
|
46,970 |
|
Intangible asset amortization expense |
|
26,557 |
|
|
20,687 |
|
|
|
105,252 |
|
|
82,823 |
|
Estimated income tax impact from adjustments and other items |
|
(4,902 |
) |
|
(5,272 |
) |
|
|
(48,792 |
) |
|
(37,573 |
) |
Total of non-GAAP adjustments |
|
53,821 |
|
|
49,264 |
|
|
|
203,884 |
|
|
180,036 |
|
Adjusted net income |
$ |
73,256 |
|
|
69,098 |
|
|
$ |
196,940 |
|
|
247,777 |
|
|
|
|
|
|
|
|
|
Adjusted diluted net income per share |
|
0.97 |
|
|
0.89 |
|
|
$ |
2.56 |
|
|
3.10 |
|
Weighted average common shares outstanding for diluted net income
per share |
|
76,419 |
|
|
77,959 |
|
|
|
77,079 |
|
|
80,337 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
INTEGRA LIFESCIENCES
HOLDINGS CORPORATION CONDENSED BALANCE SHEET DATA (UNAUDITED) |
|
|
|
|
(In thousands) |
|
|
|
|
|
|
|
|
December 31, |
|
December 31, |
|
2024 |
|
2023 |
|
|
|
|
Cash and cash equivalents |
$ |
246,375 |
|
|
$ |
276,402 |
|
Accounts receivable, net |
|
272,370 |
|
|
|
259,327 |
|
Inventory, net |
|
429,090 |
|
|
|
389,608 |
|
|
|
|
|
Current and long-term borrowing under senior credit facility |
$ |
1,121,823 |
|
|
|
840,094 |
|
Borrowings under securitization facility |
|
108,100 |
|
|
|
89,200 |
|
Convertible securities |
|
573,170 |
|
|
|
570,255 |
|
|
|
|
|
Stockholders' equity |
|
1,545,280 |
|
|
|
1,587,884 |
|
|
|
|
|
|
|
|
|
INTEGRA LIFESCIENCES HOLDINGS CORPORATION CONDENSED STATEMENT OF
CASH FLOWS (UNAUDITED) |
|
|
|
Twelve Months Ending December 31, |
|
2024 |
2023 |
Net cash provided by operating activities |
$ |
129,382 |
|
$ |
139,955 |
|
Net cash used in investing activities |
|
(390,808 |
) |
|
(94,178 |
) |
Net cash used in by financing activities |
|
237,863 |
|
|
(229,925 |
) |
Effect of exchange rate changes on cash and cash equivalents |
|
(6,464 |
) |
|
3,889 |
|
|
|
|
Net increase (decrease) in cash and cash equivalents |
|
(30,027 |
) |
|
(180,259 |
) |
|
|
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - GAAP OPERATING CASH FLOW
TO MEASURES OF ADJUSTED FREE CASH FLOW AND ADJUSTED FREE CASH FLOW
CONVERSION (UNAUDITED) |
|
|
(In thousands) |
|
|
|
|
Three Months Ended December 31, |
|
2024 |
2023 |
GAAP Net cash provided by operating activities |
$ |
50,746 |
|
$ |
58,746 |
|
|
|
|
Purchases of property and equipment |
|
(29,599 |
) |
|
(24,563 |
) |
Adj. Free Cash Flow |
$ |
21,147 |
|
$ |
34,183 |
|
|
|
|
Adjusted net income (1) |
$ |
73,256 |
|
|
69,098 |
|
Adjusted Free Cash Flow Conversion |
|
28.8 |
% |
|
49.5 |
% |
|
|
|
|
|
|
|
Twelve Months Ending December 31, |
|
2024 |
2023 |
GAAP Net cash provided by operating activities |
$ |
129,382 |
|
$ |
139,955 |
|
|
|
|
Purchases of property and equipment |
|
(104,418 |
) |
|
(66,865 |
) |
Adj. Free Cash Flow |
$ |
24,964 |
|
$ |
73,090 |
|
|
|
|
Adjusted net income (1) |
$ |
196,940 |
|
|
247,777 |
|
Adjusted Free Cash Flow Conversion |
|
12.7 |
% |
|
29.5 |
% |
|
|
|
(1) Adjusted net income for quarters and twelve
months ended December 31, 2023 and 2024 are reconciled above.
Adjusted net income for remaining quarters in the trailing twelve
months calculation have been previously reconciled and are publicly
available in the Quarterly Earnings Call Presentations on our
website at investor.integralife.com.
The Company calculates adjusted free cash flow
conversion by dividing its free cash flow by adjusted net income.
The Company believes this measure is a useful metric in evaluating
the significance of the cash special charges in its adjusted
earnings measures.
|
|
RECONCILIATION OF NON-GAAP ADJUSTMENTS - NET DEBT CALCULATION
(UNAUDITED) |
|
|
(In thousands) |
|
|
December 31, 2024 |
December 31, 2023 |
Short-term borrowings under senior credit facility |
$ |
33,906 |
|
$ |
14,531 |
|
Long-term borrowings under senior credit facility |
|
1,087,917 |
|
|
825,563 |
|
Borrowings under securitization facility |
|
108,100 |
|
|
89,200 |
|
Convertible Securities |
|
573,170 |
|
|
570,255 |
|
Deferred financing costs netted in the above |
|
5,475 |
|
|
9,651 |
|
Short-term investments |
|
(27,192 |
) |
|
(32,694 |
) |
Cash & Cash Equivalents |
|
(246,375 |
) |
|
(276,402 |
) |
Net Debt |
$ |
1,535,001 |
|
$ |
1,200,104 |
|
|
|
|
Integra LifeSciences (NASDAQ:IART)
과거 데이터 주식 차트
부터 2월(2) 2025 으로 3월(3) 2025
Integra LifeSciences (NASDAQ:IART)
과거 데이터 주식 차트
부터 3월(3) 2024 으로 3월(3) 2025