# Hosmer Dorrance Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1977–1982): 9 510(k) clearances
- Product codes: IQI (3), ION (2), IRE (1), ITS (1), IQX (1), ITQ (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
- K822632: Elbow Prosthesis (Sep 14, 1982)
- K821704: Fracture Bracing (Jun 24, 1982)
- K801788: Humerous Fracture Brace, Ulna Fracture (Aug 7, 1980)
- K780891: Post-Operative Hip Orthosis (Jun 13, 1978)
- K780890: Capp Terminal Device (Jun 13, 1978)
- K780892: Fracture Bracing (Jun 13, 1978)
- K761312: Orthotic Bracing (Jan 10, 1977)
- K761313: 4-Bar Knee-Shin Set-UP (Jan 10, 1977)

Source page: https://510kreport.com/company/hosmer-dorrance