# Univec, Inc.

- Location (FDA's records): Garden City, NY
- FDA decisions: 7 (1994–2002): 7 510(k) clearances
- Product codes: FMI (2), MEG (2), FMF (2), SCL (1)
- Predicates its devices cite: 3 (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
- Flp Ent., Inc.: 1 (https://510kreport.com/company/flp-ent)

## Its most-cited devices
- K943679: Univec Nonresusable Locking Syringe (1994), cited by 2

## Recent decisions
- K020500: Univec Bifurcated Sliding Sheath Syringe (Mar 19, 2002)
- K993996: Univec Auto-Disable Hypodermic Syringe (Jul 17, 2000)
- K000747: Univec Two Piece Syringe (Jun 8, 2000)
- K961877: Piston Syringe (Aug 7, 1996)
- K933469: Univec Non-Reusable Syringe (Apr 18, 1996)
- K951619: Univec Nonreusable Locking Syringe (Jun 6, 1995)
- K943679: Univec Nonresusable Locking Syringe (Dec 12, 1994)

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