Energy Life Systems Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Energy Life Systems Corp. makes
Energy Life Systems Corp. manufactures urologic laser fibers and reusable fiberoptic cables designed for minimally invasive procedures, including side-firing refractive fibers for precise tissue treatment and laser catheters for endoscopic applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Urotek Re-Usable Fiberoptic Cable Ref K951933
Regimes: 510(k) Registry: 510(k)Urotek Laser Catheter Ref K945560
Regimes: 510(k) Registry: 510(k)Urotek Laser Catheter Ref K934389
Regimes: 510(k) Registry: 510(k)Side-Firing Urologic Refractive Fiber Ref K943409
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Energy Life Systems Corp. have in the registry?
The registry currently lists 5 devices for Energy Life Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Energy Life Systems Corp.'s devices?
Among its 5 most recently registered devices, Energy Life Systems Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Energy Life Systems Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Energy Life Systems Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Energy Life Systems Corp. in the registry?
The most recently registered devices listed for Energy Life Systems Corp. include CONVERTIBLE CONTACT SIDE-FIRING REFRACTIVE FIBER (C-SRF(TM)), UROTEK RE-USABLE FIBEROPTIC CABLE, UROTEK LASER CATHETER and SIDE-FIRING UROLOGIC REFRACTIVE FIBER.