Data / Medical devices / Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy / United States
FDA-registered makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy (product code NHN). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
- Product code
- NHN
- Country
- United States
Makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Erchonia Corporation | Fountain Inn, SC, United States | Complaint file establishment, Manufacturer, Remanufacturer | 10 | September 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Medical Quant Usa | Solon, OH, United States | Manufacturer, Repackager or relabeler | 3 | May 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Microlight Corporation Of America | Missouri City, TX, United States | Specification developer | 1 | February 6, 2002 | 0 | 0 | 0 | api.fda.gov |
| Hair Laser Manufacturing, LLC | Southlake, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ITI Manufacturing Inc. | Sugar Land, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laser Health Technologies | Paradise Valley, AZ, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.