# Technidyne Corp.

- Location (FDA's records): Edison, NJ
- FDA decisions: 2 (1993–1993): 2 510(k) clearances
- Product codes: GGP (1), JPA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- International Technidyne Corp.: 1 (https://510kreport.com/company/international-technidyne)

## Its most-cited devices
- K930068: Hemochron Model 8000/Factor VI Premier Coagulation (1993), cited by 1

## Recent decisions
- K930235: Hemochron/Factor VI Whole Blood Factor Viii Assay (Sep 2, 1993)
- K930068: Hemochron Model 8000/Factor VI Premier Coagulation (Sep 2, 1993)

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