Logotype for Integra LifeSciences Holdings Corporation

Integra LifeSciences (IART) Q1 2025 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Integra LifeSciences Holdings Corporation

Q1 2025 earnings summary

8 Jul, 2026

Executive summary

  • Q1 2025 revenue reached $382.7 million, up 3.7% year-over-year, but organic revenue declined 3.5% due to ship holds and supply disruptions; net loss widened to $25.3 million ($0.33/share) primarily from operational and quality issues.

  • Adjusted EPS was $0.41, down 25% year-over-year, and adjusted gross margin fell 220bps to 62.2%; GAAP gross margin declined to 50.8%.

  • The company is executing a turnaround with a new transformation office, key leadership hires, and ongoing investments in compliance and supply reliability.

  • Progress continues on the Compliance Master Plan, with most manufacturing site assessments completed and remediation actions ongoing.

  • Special charges of $42.6 million in Q1 2025 included costs for acquisitions, structural optimization, and the Boston recall/Braintree transition.

Financial highlights

  • Q1 2025 reported revenue: $382.7 million (+3.7%); organic revenue: $355.8 million (-3.5%).

  • Adjusted EBITDA margin: 16.6% (down 290bps); adjusted gross margin: 62.2% (down 220bps); GAAP gross margin: 50.8%.

  • Net loss: $25.3 million; adjusted net income: $31.7 million (down 26.3%).

  • Operating cash flow: $(11.3) million; free cash flow: $(40.2) million due to higher capex.

  • Net debt at quarter-end: $1.58 billion; total liquidity: $1.16 billion.

Outlook and guidance

  • Q2 2025 revenue expected at $390–$400 million (reported decline 6.8%–4.4%, organic decline 7.5%–5.1%).

  • Full-year 2025 revenue guidance reaffirmed at $1.65–$1.72 billion; adjusted EPS guidance lowered to $2.19–$2.29 due to $0.22 per share tariff impact.

  • Ship holds for 2025 now projected at $55–$70 million, up from $27 million previously, but within the $90–$150 million disruption range.

  • Braintree facility expected operational with FDA approval in H1 2026, supporting key product launches.

  • Management plans to maintain covenant compliance through expense reductions, price increases, and operational initiatives.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more