Medical Device Manufacturer · US , Cambridge , MA

Lightforce Orthodontics

3 submissions · 3 cleared · Since 2020
3
Total
3
Cleared
0
Denied

Lightforce Orthodontics — FDA 510(k) Submissions

Lightforce Orthodontics has submitted 3 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

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

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