# Midwest Orthodontic Mfg.

- Location (FDA's records): Columbus, IN
- FDA decisions: 7 (1990–1998): 7 510(k) clearances
- Product codes: DYH (4), EJF (1), KLE (1), DYW (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
- K981433: Orthodontic Braces (Jun 25, 1998)
- K955740: Gluflorma (Feb 8, 1996)
- K952856: Light-Cure PC (Sep 12, 1995)
- K952855: PC-Lock (Sep 8, 1995)
- K952858: Light-Cure (Sep 5, 1995)
- K952857: Pro-Lock (Sep 5, 1995)
- K900824: Fluor-I-Chains (TM) and Fluor-I-Ties (TM) (May 22, 1990)

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