Manufacturer registered with FDA

Jiangsu Yongfa Medical Equipment Technology Co. Ltd.

Zhangjiagang City, China. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10070970Manufacturer
Device types listed
1
Brands and models
3
510(k) clearances
0as applicant
Markets registered in
48 registrations outside the US
Establishments
1China

Registered in 4 markets

Where regulators' registries name Jiangsu Yongfa Medical Equipment Technology Co. Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedEuropean Union: 6 registrationsColombia: 1 registrationsTanzania: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerJiangsu Yongfa Medical Equipment Technology Co. Ltd.1 device types—Below
European UnionEUDAMEDManufacturerJiangsu Yongfa Medical Equipment Technology Co. Ltd.6—Pure Global AI
ColombiaINVIMAManufacturerJIANGSU YONGFA MEDICAL EQUIPMENT TECHNOLOGY CO., LTD.1—Pure Global AI
TanzaniaTMDAManufacturerJIANGSU YONGFA MEDICAL EQUIPMENT TECHNOLOGY CO., LIMITED12025–2025Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Jiangsu Yongfa Medical Equipment Technology Co. Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Suction Operatory UnitEBR · Class 1Suction & evacuation unitsMaker
Electric Suction UnitManual Suction UnitSputum Suction Unit
2023

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
JIANGSU YONGFA MEDICAL EQUIPMENT TECHNOLOGY CO., LTDFDA reg. 3017181414Zhangjiagang City Jiangsu, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10070970). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.