Not currently registered with FDA under this name

Neosil Co., Ltd.

Gyeongsangnam-Do, South Korea. Named as applicant on 2 dental 510(k) clearances between 2015 and 2018. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
22015–2018
Markets registered in
43 registrations outside the US
Establishments
0—
2015: 12018: 120102020

510(k) clearances per year, 2007–2026

Registered in 4 markets

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

All markets
United States: 2 clearancesAustralia: 1 registrationsColombia: 1 registrationsTaiwan: 1 registrations
RegisteredHome: South KoreaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantNeosil Co., Ltd.2 clearances2015–2018Below
AustraliaTGAManufacturerNeosil Co Ltd12015–2015Pure Global AI
ColombiaINVIMAManufacturerNEOSIL CO LTD.1—Pure Global AI
TaiwanTFDAManufacturerNEOSIL Co., Ltd.12021–2021Pure 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 Neosil Co., Ltd. as the applicant.

Decided510(k)DeviceDevice type
13 Jun 2018K180565PEAK NS033CF, PEAK NS017CFELW Impression Material
22 Oct 2015K152180PEAKELW Impression 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.