# American Design Group, Inc.

- Location (FDA's records): Concord, CA
- FDA decisions: 3 (1989–1991): 3 510(k) clearances
- Product codes: LZN (2), GDM (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K911717: Adg Intramedullary Bone Plug - Vented (Sep 4, 1991)
- K902615: Adg Bone Plug (Sep 11, 1990)
- K890722: Adg Bone Biopsy System (Sep 21, 1989)

Source page: https://510kreport.com/company/american-design-group