Ascon Medical Instruments, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ascon Medical Instruments, Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Ascon Medical Instruments, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Westmont, US.
Historical record: 6 cleared submissions from 1985 to 1985. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ascon Medical Instruments, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ascon Medical Instruments, Ltd.
6 devices
Cleared
Sep 05, 1985
CONTACT LENS LOUPE, INSPETION LOUPE
Ophthalmic
119d
Cleared
Sep 04, 1985
ASCON OPHTHALMIC SPONGE
Ophthalmic
118d
Cleared
Jul 31, 1985
ATL 225 MW TRAIL LENS SET
Ophthalmic
49d
Cleared
Jun 27, 1985
ASCON SURGICAL INSTRUMENTS
Ophthalmic
49d
Cleared
Jun 05, 1985
ACC CROSS CYLINDERS
Ophthalmic
27d
Cleared
Jun 05, 1985
ATF 101 TRAIL FRAME
Ophthalmic
21d