Solidex? Ti-Links and Screws
Feb 2026
270d
CreoDent Hudson Valley
1
Total
1
Cleared
0
Denied
CreoDent Hudson Valley — FDA 510(k) Submissions
CreoDent Hudson Valley has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Abutment, Implant, Dental, Endosseous . Use the specialty filter in the sidebar to narrow results.
1 devices