Not currently registered with FDA under this name

B&Medi Co., Ltd.

Incheon, South Korea. Named as applicant on 1 dental 510(k) clearance between 2022 and 2022. 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
12022–2022
Markets registered in
32 registrations outside the US
Establishments
0—
2022: 120102020

510(k) clearances per year, 2007–2026

Registered in 3 markets

Where regulators' registries name B&Medi Co., Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesIsrael: 1 registrationsTaiwan: 1 registrations
RegisteredHome: South KoreaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantB&Medi Co., Ltd.1 clearances2022–2022Below
IsraelAMARManufacturerB&Medi Co., Ltd.1—Pure Global AI
TaiwanTFDAManufacturerB&Medi Co., Ltd.12019–2019Pure 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 B&Medi Co., Ltd. as the applicant.

Decided510(k)DeviceDevice type
18 Aug 2022K210797Bio-MEM Ti Reinforced MembraneNPK Intraoral Synthetic Barrier

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.