Visioncare Devices, Inc.
Visioncare Devices, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 10, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K212763 | UniVit HE, UniVit UHS | August 10, 2022 |
| K120170 | PROCARE PLUS VITRECTOMY SYSTEM | May 30, 2012 |
| K023939 | VELOCITY ADVANTAGE | April 17, 2003 |
| K971064 | BAYERS BIMANUAL I/A HANDPIECES | June 9, 1997 |
| K940746 | VIT CUTTER MODEL 94 | June 6, 1994 |
| K904909 | I/A VITROPHAGE MODEL YPR 2001 | January 28, 1991 |