# Surgeon Surgical Instrumentation, Inc.

- Location (FDA's records): Placentia, CA
- FDA decisions: 10 (1983–1995): 10 510(k) clearances
- Product codes: KYG (2), GCT (1), HOY (1), GDW (1), HQC (1), GBX (1), LFL (1), HIF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Marina Medical Instruments, Inc.: 1 (https://510kreport.com/company/marina-medical-instruments)
- Tools For Surgery, LLC: 1 (https://510kreport.com/company/tools-for-surgery)

## Its most-cited devices
- K890447: Hemorrhage Occludor (1989), cited by 2

## Recent decisions
- K954241: Surgin Genisis Phacoemulsifier (Dec 1, 1995)
- K932281: Verres Needle (Aug 6, 1993)
- K922038: CO2 Insufflation Tubing (Oct 13, 1992)
- K904010: Surgical Aspirator Kit (Nov 21, 1990)
- K890447: Hemorrhage Occludor (Feb 23, 1989)
- K880543: Uni-Port (Jul 1, 1988)
- K881232: Surgin Eye Shield (Apr 13, 1988)
- K861203: Multi-Spike (Apr 28, 1986)

Source page: https://510kreport.com/company/surgeon-surgical-instrumentation