Ophthalmic Consultants, Inc. is one of 9846 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ophthalmic Consultants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: I/A (IRRIGATION/ASPIRATION) PACK, POSTERIOR VITRECOMY PACK, ANTERIOR VIRECTOMY PACK, PHACOEMULSIFICATION PACK, ADMIINISN, SCLERAL PLUGS, 19 AND 20 GAUGE
2
Total
2
Cleared
0
Denied
Ophthalmic Consultants, Inc. has 2 FDA 510(k) cleared medical devices. Based in Tooele, US.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ophthalmic Consultants, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ophthalmic Consultants, Inc.
2 devices