# Uhi Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1982–1984): 3 510(k) clearances
- Product codes: INX (2), KME (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: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K843389: Clinitron Air Fluidized Support J-101UD (Sep 5, 1984)
- K821835: Barrier Burn Sheet (Jul 2, 1982)
- K813584: Clinitron Air Fluidized Support System (Jan 12, 1982)

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