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Data / Medical devices / China / Dongguan Yingfeng Metal & Plastic Products Co., Ltd

Dongguan Yingfeng Metal & Plastic Products Co., Ltd: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance

Dongguan Yingfeng Metal & Plastic Products Co., Ltd is registered with the FDA (registration 3015977541) in Dongguan Guangdong, China. It lists 14 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 18, 2019. Registered through 2027. 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.

FDA registration number
3015977541
Address
No. 1, Road 2, Bianpu Industrial Zone, Lianhu Road, Qiaotou Town, Dongguan Guangdong, China, 523520
Owner or operator
Dongguan Yingfeng Metal & Plastic Products Co., Ltd (10061441)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
October 18, 2019
Registered through
2027
Brand names listed
AB FLEX, Ab Flex, Air Leggy, Bicit, Conductive Gel for external use, Deep Tissue Percussion Massager, Dental Polisher, EMS belt and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 18, 2019K183103EMS Belt (Model MC0485)NGXSubstantially EquivalentDongguan Yingfeng Metal & Plastic Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 18, 2019. 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.