Bone Anchorage Systems, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Bone Anchorage Systems, Inc. makes
Bone Anchorage Systems, Inc. manufactures endosseous dental implants designed for oral and maxillofacial applications, including tooth replacement and bone integration.
The company’s portfolio is regulated under FDA Class II devices and listed via 510(k) premarket notifications. The manufacturer operates from the United States.
Catalogue
Endosseous Dental Implant Ref K881924
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bone Anchorage Systems, Inc. have in the registry?
The registry currently lists 1 device for Bone Anchorage Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bone Anchorage Systems, Inc.'s devices?
Among its 1 most recently registered device, Bone Anchorage Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bone Anchorage Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bone Anchorage Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bone Anchorage Systems, Inc. in the registry?
The most recently registered devices listed for Bone Anchorage Systems, Inc. include ENDOSSEOUS DENTAL IMPLANT.