Data / Medical devices / Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy / China
FDA-registered makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy in China: 5 establishments
5 establishments in China 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). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 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
- China
Makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hubei Yjt Intelligent Technology Group Co., Ltd. | Wuhan Hubei, China | Manufacturer | 1 | February 6, 2002 | 0 | 0 | 0 | api.fda.gov |
| Rhein Laser Technologies Co., Ltd. | wuhan Hubei, China | Complaint file establishment, Manufacturer | 1 | November 25, 2003 | 0 | 0 | 0 | api.fda.gov |
| Seic Shenzhen Shinelong Electronics Industrial Co. | Long Gang District,, SHENZHEN Guangdong, China | Contract manufacturer, Exporter to the US | 1 | February 6, 2002 | 0 | 0 | 0 | api.fda.gov |
| Wuhan Guangdun Technology Co.,ltd | WUHAN Hubei, China | Manufacturer | 1 | January 24, 2025 | 0 | 0 | 0 | api.fda.gov |
| Wuhan Lotuxs Technology Co.,ltd. | Wuhan Hubei, China | Complaint file establishment, Manufacturer | 1 | November 25, 2003 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.