# Lasermatic, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 10 (1988–1991): 10 510(k) clearances
- Names in FDA's records: Lasermatic, Inc. (8); Lasermatic OY (2)
- Product codes: GEX (5), LNK (2), LLO (1), EWG (1), HHR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K903131: Lasermatic Supercombo (TM) Surgical Laser System (Feb 19, 1991)
- K901638: Modified Combolaser 5050 & New Model 5050 Ver. 33 (Jun 27, 1990)
- K895279: Lasermatic Combolaser Model 5050 (Nov 8, 1989)
- K893529: Combolaser Model 5050 (Jun 8, 1989)
- K871875: Model 5050 Surgilaser for OB-Gyn Use (Aug 22, 1988)
- K870587: Lasermatic Surgilaser Model 5050 (Aug 10, 1988)
- K871934: Model 5050 Surgilaser for Gastro-Intestinal Use (Mar 25, 1988)
- K871932: Model 5050 Surgilaser for Urology Use (Mar 25, 1988)

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