Medical Device Manufacturer · US , Wakefield , MA

Agion Technologies, LLC

1 submissions · 1 cleared · Since 2002
1
Total
1
Cleared
0
Denied

Agion Technologies, LLC — FDA 510(k) Submissions

Agion Technologies, LLC has submitted 1 FDA 510(k) premarket notifications since 2002, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices
1–1 of 1
Filters
Filter by Specialty
All1 Dental 1