Bioinfera, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Bioinfera, Inc. makes
Bioinfera, Inc. manufactures dental implant systems, including the Reliadent Dental Implant System and its modifications, designed for osseointegrated tooth replacement in oral and maxillofacial applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Modification To Reliadent Dental Implant System Ref K061323
Regimes: 510(k) Registry: 510(k)Reliadent Dental Implant System Ref K043428
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioinfera, Inc. have in the registry?
The registry currently lists 2 devices for Bioinfera, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioinfera, Inc.'s devices?
Among its 2 most recently registered devices, Bioinfera, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bioinfera, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bioinfera, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioinfera, Inc. in the registry?
The most recently registered devices listed for Bioinfera, Inc. include MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM and RELIADENT DENTAL IMPLANT SYSTEM.