EndoDrill? Model X
Mar 2023
602d
Bibbinstruments AB
1
Total
1
Cleared
0
Denied
Bibbinstruments AB — FDA 510(k) Submissions
Bibbinstruments AB has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Biopsy Needle . Use the specialty filter in the sidebar to narrow results.
1 devices