Data / Medical devices / Powered Laser Surgical Instrument With MicrobeamFractional Output / China
FDA-registered makers of Powered Laser Surgical Instrument With MicrobeamFractional Output in China: 9 establishments
9 establishments in China are registered with the FDA to make Powered Laser Surgical Instrument With MicrobeamFractional Output (product code ONG). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Powered Laser Surgical Instrument With MicrobeamFractional Output
- Product code
- ONG
- Country
- China
Makers of Powered Laser Surgical Instrument With MicrobeamFractional Output in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shanghai Apolo Medical Technology Co.,ltd. | Shanghai, China | Manufacturer | 2 | July 2, 2025 | 0 | 0 | 0 | api.fda.gov |
| Beijing Perfectlaser Technology Co.,ltd | Beijing, China | Exporter to the US, Manufacturer | 1 | July 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| Beijing Sincoheren Science & Technology Development Co., Ltd | Bejing Beijing, China | Manufacturer | 1 | July 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| Olemy Laser Technology Ltd | Wuxi Jiangsu, China | Manufacturer | 1 | November 30, 2018 | 0 | 0 | 0 | api.fda.gov |
| Sanhe Jumei Technology Co.,ltd | Sanhe Hebei, China | Exporter to the US, Manufacturer | 1 | July 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| Wingderm Electro-Optics Ltd. | Beijing, China | Exporter to the US, Manufacturer | 1 | April 30, 2020 | 0 | 1 | 0 | api.fda.gov |
| Beijing Beautemax Technology Limited | Beijing, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Winkonlaser Technology Limited | Beijing, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weifang Mingliang Electronics Co.,ltd. | Weifang Shandong, China | Manufacturer | 0 | 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.