Skip to the page

Data / Medical devices / United States / Laser Health Technologies

Laser Health Technologies: FDA-registered device maker in Paradise Valley, AZ, United States, 2 510(k) clearances

Laser Health Technologies is registered with the FDA (registration 3007719656) in Paradise Valley, AZ, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 15, 2010. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3007719656
Address
5268 E. Onyx Ave, Paradise Valley, AZ, United States, 85253
Owner or operator
Laser Health Technologies (10029538)
Roles
Repackager or relabeler, Specification developer
First device listed
May 28, 2009
Registered through
2026
Brand names listed
LaserTouchOne, LaserTouchOne (OTC)

Devices it lists

DeviceProduct codeClassRoleSource
Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain TherapyNHN2Repackager or relabeler, Specification developeraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Repackager or relabeler, Specification developeraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Repackager or relabeler, Specification developeraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 15, 2010K100116LASERTOUCHONE (OTC)NUHSubstantially EquivalentLaser Health Technologies, LLCaccessdata.fda.gov
May 6, 2009K083822LASER TOUCHONEGZJSubstantially EquivalentLaser Health Technologies, LLCaccessdata.fda.gov

Compare with other makers

Updated April 15, 2010. 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.