Vistakon, Johnson & Johnson Vision Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vistakon, Johnson & Johnson Vision Products, Inc. - FDA 510(k) Cleare...
8
Total
8
Cleared
0
Denied
Vistakon, Johnson & Johnson Vision Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 8 cleared submissions from 1995 to 2000. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vistakon, Johnson & Johnson Vision Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vistakon, Johnson & Johnson Vision Products, Inc.
8 devices
Cleared
Feb 23, 2000
VISTAKON (LENEFILCON A)SOFT(HYDROPHILIC)CONTACT LENS CLEAR AND VISIBILITY...
Ophthalmic
63d
Cleared
Feb 23, 2000
ACUVUE (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS CLEAR AND VISIBILITY...
Ophthalmic
63d
Cleared
Jun 08, 1999
VISTAKON (LENEFILCON A) SOFT (HYDROPHILIC) CONTACT LENSES, CLEAR AND...
Ophthalmic
62d
Cleared
May 06, 1999
ACUVUE (ETAFILCON A)SOFT (HYDROPHILIC) CONTACT LENSES, CLEAR AND VISIBILITY...
Ophthalmic
34d
Cleared
Jan 26, 1999
VISTAKON (LENEFILCON A)CONTACT LENS CLEAR AND VISIBILITY TINT WITH UV BLOCKER
Ophthalmic
84d
Cleared
Jan 30, 1997
VISTAKON (GENFILCON A) CONTACT LENS, CLEAR AND WITH VISIBILIITY TINT
Ophthalmic
73d
Cleared
Oct 01, 1996
ACUVUE (ETAFILCON A) CONTACT LENS CLEAR & W/VISIBILITY TINT W/UV BLOCKER
Ophthalmic
75d
Cleared
Sep 26, 1995
VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS
Ophthalmic
49d