Integra Lifescience Corportation
Country not established
- Devices
- 2
What Integra Lifescience Corportation makes
Integra Lifescience Corporation manufactures the Integra MozAIK Osteoconductive Scaffold - Strip, a device used for bone regeneration, and the Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit with Integra Camino Flex Adapter, a system for monitoring intracranial pressure.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Integra Mozaik Osteoconductive Scaffold - Strip Ref K141841
Regimes: 510(k) Registry: 510(k)Integra Camino Flex Ventricular Intracranial Pressure Monitoring Kit With Intrgra Camino Flex Adapter Ref K121159
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integra Lifescience Corportation have in the registry?
The registry currently lists 2 devices for Integra Lifescience Corportation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integra Lifescience Corportation's devices?
Among its 2 most recently registered devices, Integra Lifescience Corportation has devices listed in FDA 510(k) (2 devices).
What risk classes do Integra Lifescience Corportation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Integra Lifescience Corportation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integra Lifescience Corportation in the registry?
The most recently registered devices listed for Integra Lifescience Corportation include INTEGRA MOZAIK OSTEOCONDUCTIVE SCAFFOLD - STRIP and INTEGRA CAMINO FLEX VENTRICULAR INTRACRANIAL PRESSURE MONITORING KIT WITH INTRGRA CAMINO FLEX ADAPTER.