Not currently registered with FDA under this name

Cruxell Corp.

Daejeon, South Korea. Named as applicant on 2 dental 510(k) clearances between 2019 and 2021. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
22019–2021
Markets registered in
57 registrations outside the US
Establishments
0—
2019: 12021: 120102020

510(k) clearances per year, 2007–2026

Registered in 5 markets

Where regulators' registries name Cruxell Corp. as the manufacturer or the registration holder of a device.

All markets
United States: 2 clearancesTaiwan: 4 registrationsAustralia: 1 registrationsIsrael: 1 registrationsSerbia: 1 registrations
RegisteredHome: South KoreaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantCruxell Corp.2 clearances2019–2021Below
TaiwanTFDAManufacturerCRUXELL CORP.CRUXELL Corp.42018–2024Pure Global AI
AustraliaTGAManufacturerCruxell Corp12022–2022Pure Global AI
IsraelAMARManufacturerCRUXELL Corp.1—Pure Global AI
SerbiaALIMSManufacturerCruxell Corp.12024–2024Pure 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 Cruxell Corp. as the applicant.

Decided510(k)DeviceDevice type
29 Jul 2021K211317CRUXVIEWMUH Digital Extraoral Source X-Ray System
12 Feb 2019K183637Cruxcan (CRX-1000)MUH Digital Extraoral Source X-Ray System

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.