Annex Medical, Inc.

Annex Medical, Inc. — FDA 510(k) Submissions

Annex Medical, Inc. has submitted 23 FDA 510(k) premarket notifications since 1989, of which 23 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dislodger, Stone, Basket, Ureteral, Metal, Dislodger, Stone, Flexible, Device, Biopsy, Endomyocardial, Endoscopic Cytology Brush, Surgical Instruments, G-u, Manual (and Accessories) . Use the specialty filter in the sidebar to narrow results.