# L.A.S.E.R., Inc.

- Location (FDA's records): Tomball, TX
- FDA decisions: 14 (1985–1998): 14 510(k) clearances
- Product codes: GCJ (4), HET (3), GEX (3), GAD (1), HHR (1), FBQ (1), HRX (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Slt-J, Ltd.: 1 (https://510kreport.com/company/slt-j)

## Its most-cited devices
- K914197: Alloy Scalpel Handpieces (1992), cited by 1

## Recent decisions
- K983965: CO2 Laser Coupler (Dec 22, 1998)
- K950021: Reusable Trocar with Safety Sleeve (Mar 31, 1995)
- K940454: Grasping Forceps, Punches, Scissors (Mar 25, 1994)
- K931561: Trocar Sleeve (Feb 7, 1994)
- K933421: Endoscopic Instruments and Accessdories (Nov 2, 1993)
- K924844: Bulk Tissue Removal System (Oct 8, 1993)
- K932045: Disposable Insufflation Tubing (Sep 23, 1993)
- K931092: Endoscopic Retractor (Apr 30, 1993)

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