Not currently registered with FDA under this name

Guangzhou Rebornendo Medical Instrument Co., Ltd.

Guangzhou, China. Named as applicant on 1 dental 510(k) clearance between 2026 and 2026. No establishment is registered with FDA under this exact name today.

1 clearance in five years
Device types listed
0
Brands and models
0
510(k) clearances
12026–2026
Markets registered in
47 registrations outside the US
Establishments
0—
2026: 120102020

510(k) clearances per year, 2007–2026

Registered in 4 markets

Where regulators' registries name Guangzhou Rebornendo Medical Instrument Co., Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesEuropean Union: 3 registrationsTaiwan: 2 registrationsUnited Kingdom: 2 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantGuangzhou Rebornendo Medical Instrument Co., Ltd.1 clearances2026–2026Below
European UnionEUDAMEDManufacturerGuangzhou RebornEndo Medical Instrument Co., Ltd.3—Pure Global AI
TaiwanTFDAManufacturerGUANGZHOU REBORNENDO MEDICAL INSTRUMENT CO., LTD.22019–2019Pure Global AI
United KingdomMHRAManufacturerGuangzhou RebornEndo Medical instrument Co,. Ltd.2—Pure 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

510(k) clearances

Clearances on which FDA names Guangzhou Rebornendo Medical Instrument Co., Ltd. as the applicant.

Decided510(k)DeviceDevice type
18 Jun 2026K253131Curing Light (M-Cure 6)EBZ Ultraviolet Activator for Polymerization

Sources

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 of the most recent filing, which can be a US agent.