Registered with FDA

Vehu Medical Instrumente GmbH

TUTTLINGEN, Germany. Lists 19 dental device types with FDA across 1 registered establishment.

FDA owner/operator9040464Repacker / relabeler
Device types listed
19
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Germany

Devices listed with FDA

What Vehu Medical Instrumente GmbH currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Orthodontic WireDZC · Class 1Orthodontic wires & bandsLister—2009
Mouth MirrorEAX · Class 1Dental hand instrumentsLister—2000
Retentive and Splinting Pin and Accessory InstrumentsEBL · Class 1—Lister—2001
Orthodontic Wire ClampECN · Class 1—Lister—2009
Orthodontic Band SetterECR · Class 1Dental hand instrumentsLister—2001
Dental Dressing ForcepsEFL · Class 1Dental hand instrumentsLister—2001
All Types RetractorEIG · Class 1Dental hand instrumentsLister—2001
Crown RemoverEIS · Class 1Dental hand instrumentsLister—2003
Rubber Dam Clamp ForcepsEJG · Class 1Rubber dam systemsLister—2003
Operative Amalgam CarrierEKI · Class 1Dental hand instrumentsLister—2008
Surgical Biopsy PunchEME · Class 1Dental hand instrumentsLister—2000
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsLister—2001
Surgical Rongeur ForcepsEMH · Class 1Dental hand instrumentsLister—2000
Surgical Bone FileEMI · Class 1Dental hand instrumentsLister—2000
Surgical Bone ChiselEML · Class 1Dental hand instrumentsLister—2000
Surgical Osteotome ChiselEMM · Class 1Dental hand instrumentsLister—2000
Periodontic ScalerEMN · Class 1Dental hand instrumentsLister—2009
Mechanical Denture CleanerJER · Class 1Denture cleansers & adhesivesLister—2002
Orthodontic PlierJEX · Class 1Dental hand instrumentsLister—2004

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
VEHU MEDICAL INSTRUMENTE GMBHFDA reg. 9616246TUTTLINGEN Baden-Wurttemberg, GermanyRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9040464). 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.