Data / Medical devices / Hungary / Lighttech Ltd.
Lighttech Ltd.: FDA-registered device maker in DUNAKESZI Pest, Hungary, 1 510(k) clearance
Lighttech Ltd. is registered with the FDA (registration 9616478) in DUNAKESZI Pest, Hungary. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9616478
- FEI number
- 3003695041
- Address
- Hegyrejaro Ut 1, DUNAKESZI Pest, Hungary, 2120
- Owner or operator
- LIGHTTECH LTD. (9035094)
- Roles
- Manufacturer
- First device listed
- September 21, 1998
- Registered through
- 2026
- Brand names listed
- Sunfit Lamps for Tanning, UV Lamps For Indoor Tanning Devices
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Booth, Sun Tan | LEJ | 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 |
|---|---|---|---|---|---|---|
| December 17, 2015 | K151370 | UV Lamps for Indoor Tanning Devices | LEJ | Substantially Equivalent | Light Sources, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 17, 2015. 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.