Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006999111

FEI Number

3006999111

Entity Name

MERZ PHARMA GMBH & CO. KGAA

City/State/Country

Reinheim Hesse, DE

Establishment Address

Ludwigstrasse 22, Reinheim Hesse 64354, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Merz Pharma GmbH & Co. KGaA (Owner Number: 10060155)

Owner / Operator Contact Address

Ludwigstrasse 22, Reinheim, DE-NOTA 64354, 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
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2019-04-11

Official Correspondent

Torben Weilmuenster

US Agent Details

Micki Lew Business: Merz North America Email: micki.lew@merz.com Phone: (919) 6915943

Related Public Records

Same Entity

Merz Pharma GmbH & Co. KGaA

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 3006999111. Last updated year: 2026. Please use registration number 3006999111 when referencing this establishment in official correspondence.