# Laser Media

- Location (FDA's records): Hauppauge, NY
- FDA decisions: 13 (1985–1987): 12 510(k) clearances and 1 original PMA approval
- Product codes: LNK (8), LLO (2), HHR (2), LOI (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
- K872352: Fiberlase II ND:Yag Laser for Treat of Menorrhagia (Dec 30, 1987)
- K872351: Fiberlase II ND:Yag Laser for Pulmonary Use (Dec 11, 1987)
- K872350: Fiberlase II ND:Yag Laser for Gastro.&Urology Use (Aug 10, 1987)
- K872031: Uni-Fiber Non-Repairable Fiber Delivery System (Aug 4, 1987)
- K863428: Single Use Laser Fiber Delivery System for ND: Yag (Dec 3, 1986)
- K863583: Change in Fiberlase 100 ND:Yag Medical Laser (Nov 24, 1986)
- K862444: Fiberlase 100 Medical Laser Sys/ND:Yag Menorrhagia (Sep 25, 1986)
- K860063: ND:Yag Laser Single Use Fiber Delivery System (Feb 5, 1986)

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