Cantor & Silver , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cantor & Silver , Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cantor & Silver , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 4 cleared submissions from 1998 to 2000. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Cantor & Silver , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cantor & Silver , Ltd.
4 devices
Cleared
Oct 20, 2000
CHROMAGEN V2.0 HAPLOSCOPIC SYSTEM & COLOR VISION ENHANCEMENT SOFT CONTACT LENSES
Ophthalmic
303d
Cleared
Aug 18, 1999
CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT...
Ophthalmic
23d
Cleared
Apr 21, 1999
CANTOR & SILVER 5X TINTED (HIOXIFILCON A) SOFT (SPHERICAL & TORIC) DAILY WEAR...
Ophthalmic
44d
Cleared
Jun 24, 1998
CANTOR & SILVER 5X (HIOXIFILCON A) SOFT (SPHERICAL & TORIC) DAILY WEAR...
Ophthalmic
35d