# American Midwest

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1980–1982): 5 510(k) clearances
- Product codes: EBF (2), EFB (1), EBZ (1), EGS (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
- K821895: AH-1 Light-Cure Dental Composite Restor (Jul 16, 1982)
- K821715: AM-40 System (Jun 25, 1982)
- K820693: Midwest Light Wand (Apr 9, 1982)
- K811979: Att-1 Dental Composite Restorative Sys (Aug 18, 1981)
- K800735: U-Style Adapter (Apr 10, 1980)

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