Manufacturer registered with FDA

Hermann Mueller Medizintechnik GmbH

TUTTLINGEN, Germany. Lists 9 dental device types with FDA across 1 registered establishment.

FDA owner/operator9010992Contract manufacturerManufacturer
Device types listed
9
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Germany

Devices listed with FDA

What Hermann Mueller Medizintechnik GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
All Types RetractorEIG · Class 1Dental hand instrumentsMaker—1994
Dental Wax CarverEIK · Class 1Dental hand instrumentsMaker—2013
Dental Plastic Filling InstrumentEIY · Class 1Dental hand instrumentsMaker
VARIOUS TYPES OF DEN
1994
Operative ExplorerEKB · Class 1Dental hand instrumentsMaker—2013
Operative Dental ExcavatorEKC · Class 1Dental hand instrumentsMaker—2013
Endodontic Root Canal PluggerEKR · Class 1Dental hand instrumentsMaker—2013
Surgical Bone FileEMI · Class 1Dental hand instrumentsMaker—2013
Dental Surgical ElevatorEMJ · Class 1Dental hand instrumentsMaker—1997
Surgical Osteotome ChiselEMM · Class 1Dental hand instrumentsMaker—1997

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
HERMANN MUELLER Medizintechnik GmbHFDA reg. 9680735TUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9010992). 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.