# Visioncare Devices, Inc.

- Location (FDA's records): Redding, CA
- FDA decisions: 6 (1991–2022): 6 510(k) clearances
- Names in FDA's records: Visioncare Devices, Inc. (5); Visioncare Devices, LLC (1)
- Product codes: HQE (5), HQC (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Syntec, Inc.: 1 (https://510kreport.com/company/syntec)
- Visitec Co.: 1 (https://510kreport.com/company/visitec)

## Its most-cited devices
- K120170: Procare Plus Vitrectomy System (2012), cited by 1
- K904909: I/a Vitrophage Model Ypr 2001 (1991), cited by 1

## Recent decisions
- K212763: UniVit HE, UniVit UHS (Aug 10, 2022)
- K120170: Procare Plus Vitrectomy System (May 30, 2012)
- K023939: Velocity Advantage (Apr 17, 2003)
- K971064: Bayers Bimanual I/a Handpieces (Jun 9, 1997)
- K940746: Vit Cutter Model 94 (Jun 6, 1994)
- K904909: I/a Vitrophage Model Ypr 2001 (Jan 28, 1991)

Source page: https://510kreport.com/company/visioncare-devices