# Orthotech

- Location (FDA's records): Tampa, FL
- FDA decisions: 2 (1994–1997): 2 510(k) clearances
- Product codes: EJF (1), HTY (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Kirschner Medical Corp.: 1 (https://510kreport.com/company/kirschner-medical)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)

## Recent decisions
- K971453: Orthotec K-Cap System (Jun 24, 1997)
- K933080: Orthotech Dura-Gold Barckets (Mar 23, 1994)

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