# Energy Life Systems Corp.

- Location (FDA's records): Costa Mesa, CA
- FDA decisions: 5 (1994–1995): 5 510(k) clearances
- Product codes: GEX (5)
- 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
- K951933: Urotek RE-Usable Fiberoptic Cable (May 26, 1995)
- K945560: Urotek Laser Catheter (Jan 18, 1995)
- K945563: Convertible Contact Side-Firing Refractive Fiber (C-SRF (TM)) (Dec 15, 1994)
- K943409: Side-Firing Urologic Refractive Fiber (Aug 23, 1994)
- K934389: Urotek Laser Catheter (Feb 3, 1994)

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