company
Integra LifeSciences Corp. (NeuroSciences)
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-05-20Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product…
- fda_recall · device_recall2026-04-29Integra LifeSciences Corp. (NeuroSciences) — Class II recall: CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical asp…
- fda_recall · device_recall2026-04-22Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
- fda_recall · device_recall2026-04-22Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
- fda_recall · device_recall2026-04-22Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.
- fda_recall · device_recall2026-04-22Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.
- fda_recall · device_recall2026-04-22Integra LifeSciences Corp. (NeuroSciences) — Class II recall: Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Frequently asked questions
- How many FDA warning letters has Integra LifeSciences Corp. (NeuroSciences) received?
- Argus HQ has not recorded an FDA warning letter for Integra LifeSciences Corp. (NeuroSciences) in our current dataset.
- What FDA recalls has Integra LifeSciences Corp. (NeuroSciences) issued?
- Argus HQ has recorded 7 FDA recalls tied to Integra LifeSciences Corp. (NeuroSciences).
- Is Integra LifeSciences Corp. (NeuroSciences) FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 7 recalls, and 0 approval records for Integra LifeSciences Corp. (NeuroSciences). Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.