Data / Medical devices / United States / LiteCure, LLC
LiteCure, LLC: FDA-registered device maker in Fort Worth, TX, United States, 5 510(k) clearances
LiteCure, LLC is registered with the FDA (registration 3026668625) in Fort Worth, TX, United States. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 22, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026668625
- Address
- 3300 Eagle Parkway Suite 170, Fort Worth, TX, United States, 76177
- Owner or operator
- LITECURE, LLC (9097724)
- Roles
- Manufacturer
- First device listed
- December 22, 2010
- Registered through
- 2026
- Brand names listed
- General Surgical Laser, Medical Laser Series
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis | PDZ | 2 | Manufacturer | accessdata.fda.gov |
| 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 |
|---|---|---|---|---|---|---|
| February 22, 2018 | K173067 | LightForce LTS Model 1000, 1500, 2500, and 4000 | GEX | Substantially Equivalent | Litecure, LLC | accessdata.fda.gov |
| March 29, 2013 | K123014 | LITECURE THERAPY SYSTEM MODEL LTS-1500 | PDZ | Substantially Equivalent | Litecure, LLC | accessdata.fda.gov |
| June 12, 2012 | K121487 | LITECURE THERAPY COMPACT | ILY | Substantially Equivalent | Litecure, LLC | accessdata.fda.gov |
| January 25, 2011 | K103511 | LITECURE THERAPY SYSTEM | ILY | Substantially Equivalent | Litecure, LLC | accessdata.fda.gov |
| May 12, 2010 | K093087 | BWF-5 MEDICAL LASER SERIES | GEX | Substantially Equivalent | Litecure, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
- All makers of Powered Laser Surgical Instrument
Updated February 22, 2018. 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.