Medical Device Manufacturer · US , Washington , DC

Redent-Nova , Ltd.

3 submissions · 3 cleared · Since 2010
3
Total
3
Cleared
0
Denied

Redent-Nova , Ltd. — FDA 510(k) Submissions

Redent-Nova , Ltd. has submitted 3 FDA 510(k) premarket notifications since 2010, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Handpiece, Air-powered, Dental, Handpiece, Air-powered, Root Canal Irrigation, Handpiece, Belt And/or Gear Driven, Dental . Use the specialty filter in the sidebar to narrow results.

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