# Mnlase, Inc.

- Location (FDA's records): Reston, VA
- FDA decisions: 22 (1992–1994): 22 510(k) clearances
- Product codes: GEX (17), JRM (4), LHC (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
- K944630: Model 230-Sas Laser Delivery Probe (Nov 9, 1994)
- K944470: Curved Endophotocoagulator Laser Probe (Nov 3, 1994)
- K944626: Model 210-as Aspirating Endophotocoagulator Laser (Nov 3, 1994)
- K944628: Model 220-SS Laser Delivery Probe (Nov 3, 1994)
- K944625: Model 210-AC Aspirating Endophotocoagulator Laser (Nov 3, 1994)
- K944629: Model 230-Sac Laser Delivery Probe (Nov 3, 1994)
- K944471: Straight Endophotocoagulator Laser Probe (Nov 3, 1994)
- K944627: Model 220-SC Curved Endophotocoagulator Laser (Nov 3, 1994)

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