Medical Device Manufacturer · US , Las Vegas , NV

Oracrew

1 submissions · 1 cleared · Since 2016
1
Total
1
Cleared
0
Denied

Oracrew — FDA 510(k) Submissions

Oracrew has submitted 1 FDA 510(k) premarket notifications since 2016, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Bracket, Plastic, Orthodontic . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Dental 1