Cantor & Nissel , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cantor & Nissel , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Cantor & Nissel , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 3 cleared submissions from 2002 to 2004. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Cantor & Nissel , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cantor & Nissel , Ltd.
3 devices
Cleared
Jul 30, 2004
CANTOR & NISSEL HAND PAINTED PROSTHETIC SOFT CONTACT LENS FOR DAILY WEAR
Ophthalmic
38d
Cleared
Oct 07, 2002
CHROMAGEN V3.0 READING AID & COLOR DISCRIMINATION ENHANCEMENT SPECTACLE LENS
Ophthalmic
77d
Cleared
May 09, 2002
CHROMAGEN V3.0 READING AID SOFT CONTACT LENS
Ophthalmic
304d