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Data / Medical devices / Negative Pressure Wound Therapy Powered Suction Pump / China

FDA-registered makers of Negative Pressure Wound Therapy Powered Suction Pump in China: 7 establishments

7 establishments in China are registered with the FDA to make Negative Pressure Wound Therapy Powered Suction Pump (product code OMP). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.

Device
Negative Pressure Wound Therapy Powered Suction Pump
Product code
OMP
Country
China

Makers of Negative Pressure Wound Therapy Powered Suction Pump in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Devon Medical Products (jiangsu) LtdNantong Jiangsu, ChinaManufacturer7June 9, 2015000api.fda.gov
Alleva Medical (D.G.) LtdDongguan City Guangdong, ChinaContract manufacturer, Manufacturer6March 8, 2023000api.fda.gov
Zhejiang Longterm Medical Technology Co., LTDHuzhou City Zhejiang, ChinaManufacturer3May 31, 2022000api.fda.gov
VR Medical Technology Co., Ltd.KUNSHAN Jiangsu, ChinaManufacturer2April 28, 2017000api.fda.gov
Lightstone Medical Products (ningbo) Co LtdNingbo Zhejiang, ChinaSpecification developer1December 30, 2021000api.fda.gov
Forefront Medical Technology (jiangsu) Co.,ltdChangzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Shanghai Iso Medical Products Co., Ltd.Shanghai, ChinaContract manufacturer0000api.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.