Data / Medical devices / United States / Tria Laser Inc
Tria Laser Inc: FDA-registered device maker in Livermore, CA, United States, 2 510(k) clearances
Tria Laser Inc is registered with the FDA (registration 3036240802) in Livermore, CA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 25, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036240802
- Address
- 6256 Preston Ave, Livermore, CA, United States, 94551
- Owner or operator
- TRIA LASER INC (10055374)
- Roles
- Specification developer
- First device listed
- July 14, 2017
- Registered through
- 2026
- Brand names listed
- TRIA 4X, TRIA FRX, Tria 4X, Tria SmoothBeauty
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Specification developer | accessdata.fda.gov |
| Powered Laser Surgical Instrument With MicrobeamFractional Output | ONG | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| October 25, 2013 | K130459 | TRIA FAN SYSTEM | ONG | Substantially Equivalent | Tria Beauty, Inc. | accessdata.fda.gov |
| December 23, 2009 | K090820 | TRIA HAIR REMOVAL LASER SYSTEM | GEX | Substantially Equivalent | Spectragenics, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Laser Surgical Instrument With MicrobeamFractional Output
Updated October 25, 2013. 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.