Data / Medical devices / United States / Lasetech, LLC
Lasetech, LLC: FDA-registered device maker in Lawrenceville, NJ, United States, 5 510(k) clearances
Lasetech, LLC is registered with the FDA (registration 3015730775) in Lawrenceville, NJ, United States. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated April 3, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015730775
- Address
- 11 Princess Road Ste C, Lawrenceville, NJ, United States, 08648
- Owner or operator
- LaseTech LLC (10092722)
- Roles
- Manufacturer
- First device listed
- February 10, 2025
- Registered through
- 2026
- Brand names listed
- Alexandrite Ta2 Eraser, EpiCare Alexandrite Laser, EpiCare Alexandrite Laser, Model 501-LP, EpiCare Alexandrite Laser, Model 501-LPX, EpiCare DUO Laser, Model 504-DUO, EpiCare DUO Laser, Model 504-ZTH, EpiCare YAG Laser, Model 502-YAG, EpiCare YAG Laser, Model 504-ZTHY and more
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 |
|---|---|---|---|---|---|---|
| April 3, 2012 | K113115 | EPICARE YAG | GEX | Substantially Equivalent | Light Age, Inc. | accessdata.fda.gov |
| November 3, 2009 | K091625 | EPICARE-DUO LASER SYSTEM | GEX | Substantially Equivalent | Light Age, Inc. | accessdata.fda.gov |
| September 14, 2004 | K032991 | LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX | GEX | Substantially Equivalent | Light Age, Inc. | accessdata.fda.gov |
| January 7, 1999 | K983977 | LIGHT AGE EPICARE ALEXANDRITE LASER | GEX | Substantially Equivalent | Light Age, Inc. | accessdata.fda.gov |
| February 17, 1998 | K980131 | ALEX TA2 ERASER | GEX | Substantially Equivalent | Light Age, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 3, 2012. 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.