# Tempo Technology, Inc.

- Location (FDA's records): Columbia City, IN
- FDA decisions: 3 (1990–1996): 3 510(k) clearances
- Product codes: OXO (1), IMD (1), EAP (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
- K963220: Tempra Cold Pack, Reorder NO. TC150 (Oct 10, 1996)
- K934700: Model 90P Portable Medical Diagnostic X-Ray (Mar 16, 1994)
- K896963: Trimode SP Dental Intra Oral X-Ray (Jan 22, 1990)

Source page: https://510kreport.com/company/tempo-technology