Optonol, Ltd. is one of 25852 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optonol, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EXPRESS MINI GLAUCOMA SHUNT, EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONS
2
Total
2
Cleared
0
Denied
Optonol, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Optonol, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Optonol, Ltd.
2 devices