GreenMark Biomedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What GreenMark Biomedical, Inc. makes
GreenMark Biomedical, Inc. manufactures dental diagnostic and restorative products, including a caries detection rinse and a fluoride-enhanced biorestorative material for cavity treatment.
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
LumiCare Caries Diagnostic Rinse Ref K200601
Regimes: 510(k) Registry: 510(k)CrystLCare™ PRO Biorestorative, Fluoride-Plus Ref K241568
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does GreenMark Biomedical, Inc. have in the registry?
The registry currently lists 2 devices for GreenMark Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list GreenMark Biomedical, Inc.'s devices?
Among its 2 most recently registered devices, GreenMark Biomedical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do GreenMark Biomedical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for GreenMark Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GreenMark Biomedical, Inc. in the registry?
The most recently registered devices listed for GreenMark Biomedical, Inc. include LumiCare Caries Diagnostic Rinse and CrystLCare™ PRO Biorestorative, Fluoride-Plus.