# Visitec Co.

- Location (FDA's records): Sarasota, FL
- FDA decisions: 49 (1979–1995): 49 510(k) clearances
- Product codes: HOZ (5), HMX (3), KYG (3), LZU (2), HOY (2), HQE (2), HMP (1), LXP (1), GAR (1), HNY (1), HOF (1), HNN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Visioncare Devices, Inc.: 1 (https://510kreport.com/company/visioncare-devices)

## Its most-cited devices
- K896622: Visitec Vitrectomy Unit (1990), cited by 1

## Recent decisions
- K953394: Visitec Collar Button Catheter {Griffiths} (Oct 12, 1995)
- K945114: Visitec Scleral Plug (Feb 23, 1995)
- K945738: Visiflex Ophthalmic Surgical Incise Drape (Feb 14, 1995)
- K945172: Visitec Silicone Retinal Implants/Explants (Jan 17, 1995)
- K942234: Visitec Precise-Point (Jul 12, 1994)
- K934269: Fiberoptic Illuminated Instruments (May 17, 1994)
- K940210: Visitec Eye Pad (Mar 7, 1994)
- K933872: Visi-Spear Eye Sponge (Dec 27, 1993)

Source page: https://510kreport.com/company/visitec