Visioncare Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visioncare Devices, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Visioncare Devices, Inc. has 5 FDA 510(k) cleared medical devices. Based in Redding, US.
Historical record: 5 cleared submissions from 1991 to 2012. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Visioncare Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Visioncare Devices, Inc.
5 devices
Cleared
May 30, 2012
PROCARE PLUS VITRECTOMY SYSTEM
Ophthalmic
132d
Cleared
Apr 17, 2003
VELOCITY ADVANTAGE
Ophthalmic
142d
Cleared
Jun 09, 1997
BAYERS BIMANUAL I/A HANDPIECES
Ophthalmic
77d
Cleared
Jun 06, 1994
VIT CUTTER MODEL 94
Ophthalmic
108d
Cleared
Jan 28, 1991
I/A VITROPHAGE MODEL YPR 2001
Ophthalmic
89d