Integrity Life Sciences
Country not established
- Devices
- 1
What Integrity Life Sciences makes
Integrity Life Sciences manufactures the Integrity Spinal Care System 3.0, a device designed for spinal surgical procedures, including instrumentation and fixation components for the spine.
The portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory registry. The company is based in the United States.
Catalogue
Integrity Spinal Care System 3.0 Ref K130249
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integrity Life Sciences have in the registry?
The registry currently lists 1 device for Integrity Life Sciences. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integrity Life Sciences's devices?
Among its 1 most recently registered device, Integrity Life Sciences has devices listed in FDA 510(k) (1 device).
What risk classes do Integrity Life Sciences's devices fall under?
Among its 1 most recently registered device, the classes recorded for Integrity Life Sciences's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integrity Life Sciences in the registry?
The most recently registered devices listed for Integrity Life Sciences include INTEGRITY SPINAL CARE SYSTEM 3.0.