# A.W. Showell (Surgicraft), Ltd.

- Location (FDA's records): Worcs. B97 6hf England, GB
- FDA decisions: 2 (1985–1985): 2 510(k) clearances
- Product codes: HGP (1), KWQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Surgicraft, Ltd.: 2 (https://510kreport.com/company/surgicraft)
- Clinical Innovations, Inc.: 1 (https://510kreport.com/company/clinical-innovations)
- Barnev, Ltd.: 1 (https://510kreport.com/company/barnev)

## Its most-cited devices
- K844608: Surgicraft Copeland Disposable (1985), cited by 2
- K853033: Hartshill Rect & Wires, Spinal Fixation System (1985), cited by 2

## Recent decisions
- K853033: Hartshill Rect & Wires, Spinal Fixation System (Sep 24, 1985)
- K844608: Surgicraft Copeland Disposable (May 1, 1985)

Source page: https://510kreport.com/company/aw-showell-surgicraft