# Integra Lifescience Corportation

- Location (FDA's records): Planisboro, NJ
- FDA decisions: 2 (2012–2014): 2 510(k) clearances
- Product codes: MQV (1), GWM (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (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
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)
- Johnson & Johnson Professionals, Inc.: 1 (https://510kreport.com/company/johnson-johnson-professionals)
- Camino Laboratories, Inc.: 1 (https://510kreport.com/company/camino-laboratories)
- Camino Neurocare, Inc.: 1 (https://510kreport.com/company/camino-neurocare)

## Firms that cite its devices most
- Integra LifeSciences Corporation: 2 (https://510kreport.com/company/integra-lifesciences)

## Its most-cited devices
- K121159: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Intrgra Camino Flex Adapter (2012), cited by 2

## Recent decisions
- K141841: Integra Mozaik Osteoconductive  Scaffold - Strip (Aug 1, 2014)
- K121159: Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Intrgra Camino Flex Adapter (Jul 20, 2012)

Source page: https://510kreport.com/company/integra-lifescience-corportation