Data / Medical devices / United States / Medical Energy, Inc.
Medical Energy, Inc.: FDA-registered device maker in Pensacola, FL, United States, 1 510(k) clearance
Medical Energy, Inc. is registered with the FDA (registration 1038823) in Pensacola, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 26, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1038823
- Address
- 8806 Paul Starr DR., Pensacola, FL, United States, 32514
- Owner or operator
- MEDICAL ENERGY, INC. (1038823)
- Roles
- Manufacturer
- First device listed
- March 10, 2008
- Registered through
- 2026
- Brand names listed
- LF-40 GOLD Laser System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 26, 2004 | K041419 | LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEM | GEX | Substantially Equivalent | Medical Energy, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 26, 2004. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.