# The Deca Co.

- Location (FDA's records): Costa Mesa, CA
- FDA decisions: 9 (1982–1987): 9 510(k) clearances
- Product codes: HSB (3), JEY (1), KTW (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
- K870041: Flexible Fasciculated Bone Plate (Jul 17, 1987)
- K870040: Intramedullary Nail (Mar 26, 1987)
- K863239: Fasciculated Boat Rod (Dec 24, 1986)
- K863271: Fasciculated S Rod (Dec 24, 1986)
- K863215: Fasciculated I Rod (Dec 24, 1986)
- K861183: Intramedullary Rod (Aug 11, 1986)
- K854227: Fascilulated Nail (Feb 4, 1986)
- K830087: Intramedullary Rod (Mar 1, 1983)

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