Millenium Biologix, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Millenium Biologix, Inc. makes
Millenium Biologix, Inc. manufactures resorbable medical devices, including the SKELITE Resorbable Cement Restrictor for surgical applications and the SKELITE Synthetic Resorbable Bone Void Filler for bone defect management.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Skelite Resorbable Cement Restrictor Ref K051836
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Millenium Biologix, Inc. have in the registry?
The registry currently lists 2 devices for Millenium Biologix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Millenium Biologix, Inc.'s devices?
Among its 2 most recently registered devices, Millenium Biologix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Millenium Biologix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Millenium Biologix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Millenium Biologix, Inc. in the registry?
The most recently registered devices listed for Millenium Biologix, Inc. include SKELITE RESORBABLE CEMENT RESTRICTOR and MILLENIUM'S SKELITE SYNTHETIC RESORBABLE BONE VOID FILLER.