# Stuckenbrock Medizintechnik GmbH

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 3 (2004–2018): 3 510(k) clearances
- Product codes: HRS (1), KXE (1), HWC (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Medartis AG: 1 (https://510kreport.com/company/medartis)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Avanta Orthopaedics, Inc.: 1 (https://510kreport.com/company/avanta-orthopaedics)
- Schoening & Assoc., Inc.: 1 (https://510kreport.com/company/schoening-assoc)

## Recent decisions
- K171624: IXOS Radius Plate System (Mar 29, 2018)
- K171628: HBS2 Headless Bone Screw (Jan 12, 2018)
- K042902: Herbert Ulnar Head Prosthesis System (Dec 27, 2004)

Source page: https://510kreport.com/company/stuckenbrock-medizintechnik