Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007497008

FEI Number

3007497008

Entity Name

medmix Switzerland AG

City/State/Country

Haag Sankt Gallen, CH

Establishment Address

Ruetistrasse 7, Haag Sankt Gallen 9469, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

medmix Switzerland AG (Owner Number: 10049141)

Owner / Operator Contact Address

Ruetistrasse 7, Haag, CH-SG 9469, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SYRINGE, RESTORATIVE AND IMPRESSION MATERIAL INSTRUMENTS, DENTAL HAND Micro Applicator, ZerofloX PLUGGER, ROOT CANAL, ENDODONTIC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EID	Syringe, Restorative And Impression Material	Dental	Class 1	872.4565	2022-09-22
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2015-04-20
KXR	Applicator, Resin	Dental	Class 1	872.3140	2019-12-24
EKR	Plugger, Root Canal, Endodontic	Dental	Class 1	872.4565	2019-12-24

Official Correspondent

Emilia Kedzior

US Agent Details

Joe Bradley Email: joe.bradley@medmix.com Phone: (603) 6812727

Related Public Records

Same Entity

medmix Switzerland AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007497008. Last updated year: 2026. Please use registration number 3007497008 when referencing this establishment in official correspondence.