Data / Medical devices / China / LT Technology Limited
LT Technology Limited: FDA-registered device maker in Jinqiao Export Processing Zone (South) Shanghai, China, 4 510(k) clearances
LT Technology Limited is registered with the FDA (registration 3013121972) in Jinqiao Export Processing Zone (South) Shanghai, China. It lists 3 device types. The FDA files 4 510(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
- 3013121972
- Address
- Room 106, Building 2, No. 121 Longgui Road, Jinqiao Export Processing Zone (South) Shanghai, China, 201201
- Owner or operator
- LITECURE, LLC (9097724)
- Roles
- Manufacturer
- First device listed
- January 7, 2013
- Registered through
- 2026
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 |
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.