# Syntec, Inc.

- Location (FDA's records): Winfield, MO
- FDA decisions: 3 (1997–2001): 3 510(k) clearances
- Product codes: HQC (2), MPA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (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)
- Staar Surgical Co.: 1 (https://510kreport.com/company/staar-surgical)

## Its most-cited devices
- K002932: Phacogard (2001), cited by 1
- K980480: Syntec Vitman (1998), cited by 1

## Recent decisions
- K002932: Phacogard (Jan 4, 2001)
- K980480: Syntec Vitman (May 4, 1998)
- K971338: Syntec, Inc. Disposable Bare End Fiber (May 6, 1997)

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