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Data / Medical devices / Powered Surgical Instrument For Improvement In The Appearance Of Cellulite / China

FDA-registered makers of Powered Surgical Instrument For Improvement In The Appearance Of Cellulite in China: 5 establishments

5 establishments in China are registered with the FDA to make Powered Surgical Instrument For Improvement In The Appearance Of Cellulite (product code OUP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 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.

Device
Powered Surgical Instrument For Improvement In The Appearance Of Cellulite
Product code
OUP
Country
China

Makers of Powered Surgical Instrument For Improvement In The Appearance Of Cellulite in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beijing Beautemax Technology LimitedBeijing, ChinaForeign private label distributor, Manufacturer0000api.fda.gov
Beijing Perfectlaser Technology Co.,ltdBeijing, ChinaExporter to the US, Manufacturer0000api.fda.gov
Beijing Winkonlaser Technology LimitedBeijing, ChinaForeign private label distributor, Manufacturer0000api.fda.gov
Hebei Tuosite Technology Co.,ltdShijiazhuang Hebei, ChinaManufacturer0000api.fda.gov
Sanhe Jumei Technology Co.,ltdSanhe Hebei, ChinaExporter to the US, Manufacturer0000api.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.