# Wuestec Medical, Inc.

- Location (FDA's records): Mobile, AL
- FDA decisions: 9 (1993–1999): 9 510(k) clearances
- Product codes: IYB (2), KPR (2), IXQ (1), OWB (1), IZX (1), JAA (1), KXJ (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dornier Medtech America, Inc.: 1 (https://510kreport.com/company/dornier-medtech-america)

## Its most-cited devices
- K992103: C-Quest (1999), cited by 1

## Recent decisions
- K993962: Pensil Trauma, Model WWS6100 (Dec 21, 1999)
- K992603: XRT 600 R/F, WRF 0600 (Oct 25, 1999)
- K992103: C-Quest (Sep 1, 1999)
- K981880: DX-480, Add on Digital Imager (Oct 20, 1998)
- K974240: Lightline-M (Dec 22, 1997)
- K960083: Movable Cantilevered Radiographic Table XRT 100, 200 & 300 (Jul 24, 1996)
- K955414: XRT 400 (Jul 24, 1996)
- K935123: Superstand 300 (Mar 27, 1996)

Source page: https://510kreport.com/company/wuestec-medical