# Acorn Group, Inc.

- Location (FDA's records): Walnut Creek, CA
- FDA decisions: 4 (1990–1992): 4 510(k) clearances
- Product codes: JCX (1), KWQ (1), GEX (1), CCW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Medos International SARL: 1 (https://510kreport.com/company/medos-international)

## Its most-cited devices
- K914362: Top Cervical Spine Plates & Titanium Bone Screws (1992), cited by 3

## Recent decisions
- K914362: Top Cervical Spine Plates & Titanium Bone Screws (Apr 29, 1992)
- K912905: Laryngoscope (Sep 30, 1991)
- K904126: Visiraser (Oct 30, 1990)
- K900430: Irrigation and Suction Apparatus (Jun 5, 1990)

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