Schoening & Assoc., Inc.
Country not established
- Devices
- 1
What Schoening & Assoc., Inc. makes
Schoening & Assoc., Inc. manufactures the HBS Headless Bone Screw, a fixation device used in orthopedic surgery for stable bone stabilization without protruding heads.
The HBS Headless Bone Screw is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hbs Headless Bone Screw Ref K030302
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schoening & Assoc., Inc. have in the registry?
The registry currently lists 1 device for Schoening & Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schoening & Assoc., Inc.'s devices?
Among its 1 most recently registered device, Schoening & Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Schoening & Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Schoening & Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schoening & Assoc., Inc. in the registry?
The most recently registered devices listed for Schoening & Assoc., Inc. include HBS HEADLESS BONE SCREW.