# Surgitech, Inc.

- Location (FDA's records): Oceanside, CA
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: LIH (1), IQI (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
- Skylark Device & Systems Co., Ltd.: 1 (https://510kreport.com/company/skylark-device-systems)
- Hmp 4000, Inc.: 1 (https://510kreport.com/company/hmp-4000)

## Recent decisions
- K033358: Chronic Pain Suppressor CPS-2000, Model CPS-2000 (Nov 14, 2003)
- K031576: Spartan Orthopaedic Wrist Brace, Model SCT-1 (Jul 31, 2003)

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