Manufacturer registered with FDA

M + C Schiffer GmbH

NEUSTADT, Germany. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator9027827Contract manufacturerManufacturerSpecification developer
Device types listed
3
Brands and models
3
510(k) clearances
0as applicant
Markets registered in
27 registrations outside the US
Establishments
1Germany

Registered in 2 markets

Where regulators' registries name M + C Schiffer GmbH as the manufacturer or the registration holder of a device.

All markets
United States: 3 device types listedColombia: 7 registrations
RegisteredHome: GermanyOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerM + C Schiffer GmbH3 device types—Below
ColombiaINVIMAManufacturerM+C SCHIFFER GMBHM+ C SCHIFFER GMBH · M + C SCHIFFER GMBH7—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 M + C Schiffer GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Manual ToothbrushEFW · Class 1ToothbrushesMaker
DENTIGUARD, DENTO CLINIC, GLISTER
1996
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
Philips Oral Healthcare INC
2016
Massaging PickJET · Class 1Floss & interdental cleanersMaker
Wingbrush
2017

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
M + C SCHIFFER GMBHFDA reg. 9615008NEUSTADT/WIED Rhineland-Palatinate, GermanyContract manufacturer, Manufacturer, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9027827). 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.