# Levtech, Inc.

- Location (FDA's records): Jacksonville, FL
- FDA decisions: 5 (1985–1991): 5 510(k) clearances
- Product codes: JDQ (1), HWC (1), HAX (1), HTD (1), KWP (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
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Osteonics Corp.: 1 (https://510kreport.com/company/osteonics)

## Its most-cited devices
- K850039: Halifax Spinal Clamp (1985), cited by 2

## Recent decisions
- K910128: Levtech Titanium Bone Wire (Jun 18, 1991)
- K901144: Levtech Bone Screw (Oct 10, 1990)
- K873693: Levtech Composite Traction Tongs (Feb 5, 1988)
- K874023: Levtech Clamp Applier (Nov 6, 1987)
- K850039: Halifax Spinal Clamp (May 29, 1985)

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