Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043013991

FEI Number

3043013991

Entity Name

HG MICRO INSTRUMENTE GMBH & CO. KG

City/State/Country

Wurmlingen Baden-Wurttemberg, DE

Establishment Address

Eltastr. 7, Wurmlingen Baden-Wurttemberg 78573, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

HG Micro Instrumente GmbH & Co. KG (Owner Number: 10094931)

Owner / Operator Contact Address

Eltastr. 7, Wurmlingen, DE-BW 78573, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRC	Instrument, Ent Manual Surgical	Ear, Nose, Throat	Class 1	874.4420	2026-01-07

Official Correspondent

No official correspondent registered.

US Agent Details

Anja Fair Business: KARL STORZ ENDOSCOPY-AMERICA, INC. Email: Anja.Fair@karlstorz.com Phone: (424) 2188738

Related Public Records

Same Entity

HG Micro Instrumente GmbH & Co. KG

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K143738	Intuit Medical Products, LLC	DSS Sinusplasty Balloon Catheter	2015-08-27

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2529846	MED SAVER, INC.	PHOENIXVILLE, PA, US
3003790304	GYRUS ACMI, INC.	Westborough, MA, US
9615857	INSTRUMENTARIUM SURGICAL CORP., INC.	TERREBONNE Quebec, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043013991. Last updated year: 2026. Please use registration number 3043013991 when referencing this establishment in official correspondence.