Manufacturer registered with FDA

SCHOTT CR, s.r.o.

Valasske Mezirici, Czechia. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10025265Contract manufacturer
Device types listed
1
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
22 registrations outside the US
Establishments
1Czechia

Registered in 2 markets

Where regulators' registries name SCHOTT CR, s.r.o. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedTaiwan: 2 registrations
RegisteredHome: CzechiaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSCHOTT CR, s.r.o.1 device types—Below
TaiwanTFDAManufacturerSCHOTT CR, S.R.O.Schott CR, S.R.O.22018–2018Pure 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

Devices listed with FDA

What SCHOTT CR, s.r.o. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Ultraviolet Activator for PolymerizationEBZ · Class 2Curing lightsMaker
Fiber Optic RodLight, Fiberoptic, Dental
2022

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
SCHOTT CR, S.R.O.FDA reg. 3006984716Valasske Mezirici Zlinsky Kraj, CzechiaContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10025265). 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.