# Integra Life Sciences

- Location (FDA's records): Irvine, CA
- FDA decisions: 3 (2011–2012): 3 510(k) clearances
- Product codes: MBP (1), GXQ (1), ITH (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Isotis NV: 1 (https://510kreport.com/company/isotis)
- Osteotech, Inc.: 1 (https://510kreport.com/company/osteotech)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Vax-D Medical Technologies, LLC: 1 (https://510kreport.com/company/vax-d-medical-technologies)
- Axiom Usa., Inc.: 1 (https://510kreport.com/company/axiom-usa)

## Firms that cite its devices most
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)

## Its most-cited devices
- K120600: Duragen Secure Dural Regneration Matrix (2012), cited by 1

## Recent decisions
- K120600: Duragen Secure Dural Regneration Matrix (Jun 15, 2012)
- K103248: Integrity Spinal Care System (Apr 5, 2011)
- K103742: Accell EVO3 (Formerly Accell A2I) (Mar 17, 2011)

Source page: https://510kreport.com/company/integra-life-sciences