Fenwick Hearing Instruments is one of 15039 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fenwick Hearing Instruments - FDA 510(k) Cleared Devices
Recent clearances: AIR-CONDUCTION HEARING INSTRUMENTS: MODELS = 227, 229, 232, 216, 216P, 123, 219 (MODIFY)
2
Total
2
Cleared
0
Denied
Fenwick Hearing Instruments has 2 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 2 cleared submissions from 1991 to 1996. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Fenwick Hearing Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fenwick Hearing Instruments
2 devices