Medical Device Manufacturer · US , Gainesville , FL

Osspray, Ltd.

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Osspray, Ltd. — FDA 510(k) Submissions

Osspray, Ltd. has submitted 2 FDA 510(k) premarket notifications since 2010, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Handpiece, Air-powered, Dental, Agent, Polishing, Abrasive, Oral Cavity . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Dental 2