Magnivision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Magnivision, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Magnivision, Inc. has 8 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 8 cleared submissions from 1987 to 1990. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Magnivision, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Magnivision, Inc.
8 devices
Cleared
Mar 30, 1990
ITEM #273 CONTACT LENS CASES
Ophthalmic
38d
Cleared
Mar 30, 1990
ITEM #272 MAGNIF-EYES CONTACT LENS CASE
Ophthalmic
38d
Cleared
Feb 28, 1990
CONFEES(R)+ CONTACT LENS HOLDER
Ophthalmic
70d
Cleared
Feb 28, 1990
COMFEES(R) + CON-PAK(TM) LENS CASE
Ophthalmic
70d
Cleared
Jun 23, 1989
DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283
Ophthalmic
379d
Cleared
Jun 23, 1989
ITEM #352/#CS352* CONTACT LENS CASES
Ophthalmic
141d
Cleared
Aug 10, 1987
SOFT CONTACT LENS REMOVER
Ophthalmic
42d
Cleared
Aug 04, 1987
HARD CONTACT LENS REMOVER. ITEM #289
Ophthalmic
34d