# Medical Laser, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 9 (1985–1991): 8 510(k) clearances and 1 original PMA approval
- Product codes: FET (2), GCQ (1), GEX (1), GCM (1), FED (1), LRO (1), ODF (1), LOI (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
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)
- Clarus Medical Systems, Inc.: 1 (https://510kreport.com/company/clarus-medical-systems)

## Its most-cited devices
- K913136: Laser Endoscope Disc Decompression Kits (1991), cited by 1
- K912089: Modified Series 2100 Endoscopes (1991), cited by 1

## Recent decisions
- K913136: Laser Endoscope Disc Decompression Kits (Nov 1, 1991)
- K912265: Medilase Semi-Rigid Instrod Sheath Series AE1000 (Oct 10, 1991)
- K912447: Series 5000 Endoscope Console Models 5100 and 5200 (Sep 27, 1991)
- K912089: Modified Series 2100 Endoscopes (Aug 12, 1991)
- K901464: Medilase Series 2200 Endoscope (Aug 7, 1990)
- K900894: Medilase Series 2100 Endoscope (Jun 22, 1990)
- K900380: Medilase 5010 Endoscope Console (May 15, 1990)
- K895837: Medilase System 2010L Laser Lithotriptor (Dec 14, 1989)

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