Bone Health Technologies, Inc.
Country not established
- Devices
- 4
What Bone Health Technologies, Inc. makes
Bone Health Technologies, Inc. manufactures the Osteoboost Belt, a medical device designed to support bone health through targeted stimulation or compression therapy.
The Osteoboost Belt is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Osteoboost Belt Ref DEN230015
Regimes: De Novo Registry: 510(k)
Company details
- DUNS number
- 117605727
- [email protected]
- Phone
- 1-833-466-7836
Frequently asked questions
How many devices does Bone Health Technologies, Inc. have in the registry?
The registry currently lists 4 devices for Bone Health Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bone Health Technologies, Inc.'s devices?
Among its 4 most recently registered devices, Bone Health Technologies, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Bone Health Technologies, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bone Health Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bone Health Technologies, Inc. in the registry?
The most recently registered devices listed for Bone Health Technologies, Inc. include Osteoboost Small, Osteoboost Medium, Osteoboost Large and Osteoboost Belt.