# Laser Engineering, Inc.

- Location (FDA's records): Milford, MA
- FDA decisions: 18 (1988–2022): 18 510(k) clearances
- Product codes: GEX (15), HHR (1), GCJ (1), FYD (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)

## Its most-cited devices
- K905676: MD CO2 Surgical Laser System/Gen. Surgery and Orth (1991), cited by 1

## Recent decisions
- K211605: Dual Switch (Sep 22, 2022)
- K141908: Dual Switch (Oct 22, 2014)
- K924457: Micromanipulator (May 7, 1993)
- K912247: Universal Coupler, Laparoscopic Accessory (Nov 13, 1991)
- K912347: Bipure 1000 (Sep 23, 1991)
- K910062: 02-10,001 (Aug 16, 1991)
- K911852: Compulse CO2 Surgical Laser Sys. (Jun 7, 1991)
- K905676: MD CO2 Surgical Laser System/Gen. Surgery and Orth (Apr 22, 1991)

Source page: https://510kreport.com/company/laser-engineering