# Directed Energy, Inc.

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 39 (1984–1991): 39 510(k) clearances
- Product codes: GEX (24), EWG (5), HHR (4), LNK (4), HRX (1), HQF (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
- K904930: Surgical Carbon Dioxide Laser Syst Model 20-CH (Mar 21, 1991)
- K894241: Model 20-CH W/ AR-10A/U Optical Attachment (Jun 18, 1990)
- K883738: Carbon Dioxide Laser System Model 20-CX W/Attach. (Nov 15, 1988)
- K882926: Model AU-1 Accessory Unit (Sep 9, 1988)
- K880216: Model 20C W/an AR-10A/U & RL-20A/U for Arthroscop. (Mar 4, 1988)
- K873331: Ortho. Gas Insufflator Model in-2 for Arthro. Surg (Feb 17, 1988)
- K872709: Model 20-C, RL-20A/U, OB-10A/U (Feb 2, 1988)
- K870841: Model 20-C W/BR-20A/U Attach/Model HL-3.0 OB/Gyn (Feb 2, 1988)

Source page: https://510kreport.com/company/directed-energy