# Endo Lase, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 24 (1984–1986): 24 510(k) clearances
- Product codes: GEX (7), LNK (6), HHR (3), EWG (2), LLO (1), LKW (1), KNS (1), FFS (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
- Hogan & Hartson: 1 (https://510kreport.com/company/hogan-hartson)

## Its most-cited devices
- K842810: Infrared Coagulator (1984), cited by 1

## Recent decisions
- K853900: Endo-Lase CD40 for Neurosurgery (Jun 18, 1986)
- K853878: Endo-Lase CD-100 CO2 Laser for Neurosurgery (May 2, 1986)
- K853903: Endo-Lase CD40 CO2 for Gynecology (Feb 21, 1986)
- K853876: Endo-Lse CD-100 CO2 Laser for Gynecology (Feb 21, 1986)
- K855093: Medilas 2 ND:Yag Laser Surgery System (Feb 21, 1986)
- K853877: Endo-Lase CD-100 CO2 Laser for Dermatology (Feb 19, 1986)
- K853901: Endo-Lase CD 40 for Dermatology (Feb 19, 1986)
- K853580: Medilas 2 (Feb 13, 1986)

Source page: https://510kreport.com/company/endo-lase