Manufacturer registered with FDA

Schweizer GmbH

LIPTINGEN, Germany. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator8010367Manufacturer
Device types listed
2
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
76,613 registrations outside the US
Establishments
1Germany

Registered in 7 markets

Where regulators' registries name Schweizer GmbH as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedThailand: 6,552 registrationsSouth Korea: 45 registrationsPeru: 7 registrationsTaiwan: 5 registrationsIsrael: 3 registrationsColombia: 1 registrations
RegisteredHome: GermanyOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSchweizer GmbH2 device types—Below
ThailandThai FDAManufacturerCARL TEUFEL GMBH & CO.KGCARL TEUFEL GMBH & CO. KG · Carl Teufel GmbH & Co.KG · +16,552—Pure Global AI
South KoreaMFDSManufacturerCARL TEUFEL GMBH & COCARL TEUFEL GmbH & Co. KG · CARL TEUFEL GMBH & CO. KG452001–2025Pure Global AI
PeruDIGEMIDManufacturerCARL TEUFEL GmbH & CO. KG.CARL TEUFEL GMBH & CO. KG.72011–2022Pure Global AI
TaiwanTFDAManufacturerCARL TEUFEL GMBH & CO.CARL TEUFEL GMBH & CO. KG · CARL TEUFEL GMBH & CO., · +252005–2023Pure Global AI
IsraelAMARManufacturerCarl Teufel GmbH & Co. KGCarl Teufel GmbH & Co. KG.3—Pure Global AI
ColombiaINVIMAManufacturerCARL TEUFEL GMBH & CO. KG1—Pure 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 Schweizer GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Surgical Tissue ScissorsEGN · Class 1Dental hand instrumentsMaker—1978
Collar and Crown ScissorsEIR · Class 1Dental hand instrumentsMaker—1978

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
CARL TEUFEL GMBH & CO. KGFDA reg. 9611502LIPTINGEN Baden-Wurttemberg, GermanyManufacturer

Other names on FDA records

Carl Teufel GmbH & Co.KG

Sources

FDA establishment registration & device listing (search FDA, owner/operator 8010367). 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.