Manufacturer registered with FDA

Dausch Medizintechnik GmbH

WURMLINGEN, Germany. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator8010269Contract manufacturer
Device types listed
1
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
320 registrations outside the US
Establishments
1Germany

Registered in 3 markets

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

All markets
United States: 1 device types listedSouth Korea: 16 registrationsColombia: 4 registrations
RegisteredHome: GermanyOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerDausch Medizintechnik GmbH1 device types—Below
South KoreaMFDSManufacturerDausch Medizintechnik GmbHDAUSCH MEDIZINTECHNIK GMBH161999–2026Pure Global AI
ColombiaINVIMAManufacturerDAUSCH MEDIZINTECHNIKDAUSCH MEDIZINTECHNIK GMBH4—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 Dausch Medizintechnik GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Surgical Rongeur ForcepsEMH · Class 1Dental hand instrumentsMaker—2013

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
Dausch Medizintechnik GmbHFDA reg. 8010269WURMLINGEN Baden-Wurttemberg, GermanyContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 8010269). 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.