Integrity Spine
United Statesfrom the FDA registration address FDA FEI 3010763958
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Integrity Spine makes
Integrity Spine manufactures the Integrity Spine Core System, which is a spinal surgical device.
The company is based in the US, and its portfolio consists of Class II devices that are listed in the FDA 510(k) registry.
Catalogue
Integrity Spine Core System Ref K132718
Regimes: 510(k) Registry: 510(k)The Integrity Spine Core System Ref K223043
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010763958
- Address
- 414 W Sunset Rd Ste 205, San Antonio, TX, 78209
Frequently asked questions
How many devices does Integrity Spine have in the registry?
The registry currently lists 2 devices for Integrity Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integrity Spine's devices?
Among its 2 most recently registered devices, Integrity Spine has devices listed in FDA 510(k) (2 devices).
What risk classes do Integrity Spine's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Integrity Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integrity Spine in the registry?
The most recently registered devices listed for Integrity Spine include INTEGRITY SPINE CORE SYSTEM and The Integrity Spine Core System.