Not currently registered with FDA under this name

C.E.I.B.Med

Seoul-Si, South Korea. Named as applicant on 1 dental 510(k) clearance between 2025 and 2025. 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
12025–2025
Markets registered in
25 registrations outside the US
Establishments
0—
2025: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name C.E.I.B.Med as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesSouth Korea: 5 registrations
RegisteredHome: South KoreaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantC.E.I.B.Med1 clearances2025–2025Below
South KoreaMFDSRegistration holder중앙바이오메디컬(C.E.I.B.Med)52024–2025Pure 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

510(k) clearances

Clearances on which FDA names C.E.I.B.Med as the applicant.

Decided510(k)DeviceDevice type
12 May 2025K250763ReonEBF Resin Tooth Shade Material

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.