Visioncare Devices, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K212763UniVit HE, UniVit UHSAugust 10, 2022
K120170PROCARE PLUS VITRECTOMY SYSTEMMay 30, 2012
K023939VELOCITY ADVANTAGEApril 17, 2003
K971064BAYERS BIMANUAL I/A HANDPIECESJune 9, 1997
K940746VIT CUTTER MODEL 94June 6, 1994
K904909I/A VITROPHAGE MODEL YPR 2001January 28, 1991