Lotus Prophy Angle
Nov 2022
273d
Ajk Engineering, Inc.
1
Total
1
Cleared
0
Denied
Ajk Engineering, Inc. — FDA 510(k) Submissions
Ajk Engineering, Inc. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Handpiece, Contra- And Right-angle Attachment, Dental . Use the specialty filter in the sidebar to narrow results.
1 devices