# Surgilase, Inc.

- Location (FDA's records): Warwick, RI
- FDA decisions: 19 (1985–1993): 19 510(k) clearances
- Product codes: GEX (16), LKW (1), LLO (1), LNK (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
- Omniguide Communications, Inc.: 1 (https://510kreport.com/company/omniguide-communications)
- Omniguide, Inc.: 1 (https://510kreport.com/company/omniguide)

## Its most-cited devices
- K924664: Surgilase Fiberlase CO2 Laser Waveguide (1993), cited by 2

## Recent decisions
- K932421: Surgilase/OP 15, 20, 25, 30, 40, 50 CO2 Surg. Lase (Oct 15, 1993)
- K924664: Surgilase Fiberlase CO2 Laser Waveguide (Apr 15, 1993)
- K905006: Surgilase SL 150 Surgical Laser System (Feb 21, 1991)
- K904203: Surgilase SL 50/60 Gold Surgical Laser System (Dec 7, 1990)
- K902211: Surgilase Yag 100 Surgical Laser System (Jun 29, 1990)
- K900570: Surgilase Yag 100 in Orthopedic Surgery (May 1, 1990)
- K901211: Surgilase SL50 Surgical Laser System (Apr 26, 1990)
- K901227: Surgilase CO2 Surgical Laser Systems Model SL120 (Apr 26, 1990)

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