# Mmi, Inc.

- Location (FDA's records): Southfield, MI
- FDA decisions: 3 (1984–1991): 3 510(k) clearances
- Product codes: FGD (1), HFW (1), FCE (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
- K905026: Dual Flex Non-Latex (Dec 18, 1991)
- K860445: Clamp-N-Cut (Apr 4, 1986)
- K842130: G.I. Cleansing Kit (Aug 8, 1984)

Source page: https://510kreport.com/company/mmi