Sengewald/USA, Inc.
Country not established
- Devices
- 1
What Sengewald/USA, Inc. makes
The company manufactures orthopedic implants, specifically a spinal fixation system identified by catalog number 55 66 01, designed for internal stabilization of the spine.
This product is classified as a Class II medical device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Sengewald Catalog Number 55 66 01 Ref K863323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sengewald/USA, Inc. have in the registry?
The registry currently lists 1 device for Sengewald/USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sengewald/USA, Inc.'s devices?
Among its 1 most recently registered device, Sengewald/USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sengewald/USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sengewald/USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sengewald/USA, Inc. in the registry?
The most recently registered devices listed for Sengewald/USA, Inc. include SENGEWALD CATALOG NUMBER 55 66 01.