# Luxtec Corp.

- Location (FDA's records): Sturbridge, MA
- FDA decisions: 15 (1986–1997): 15 510(k) clearances
- Product codes: EQH (3), FSP (2), FCW (2), HRX (2), FFS (1), FWC (1), HDG (1), FST (1), HQF (1), GAD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 10 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Fiber Imaging Technologies, Inc.: 1 (https://510kreport.com/company/fiber-imaging-technologies)

## Its most-cited devices
- K890716: Luxtec Aco Series 4000 Light Source (1989), cited by 1

## Recent decisions
- K973193: Luxscope (Nov 21, 1997)
- K970642: Tenoscope (May 21, 1997)
- K970562: Tenosnare (May 14, 1997)
- K950960: Reddy Illuminator (Sep 8, 1995)
- K895248: IMS5000 Illuminated Loupes (Sep 15, 1989)
- K890716: Luxtec Aco Series 4000 Light Source (Apr 26, 1989)
- K864387: Luxtec Fiberoptic Cables (May 22, 1987)
- K864382: Frazier Suction Tube (Jan 14, 1987)

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