MORCHER GMBH

FDA Device Registration & Listing · STUTTGART Baden-Wurttemberg, DE · Registration 9617458

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
9617458
FEI Number
1000447964
Entity Name
MORCHER GMBH
City/State/Country
STUTTGART Baden-Wurttemberg, DE
Establishment Address
KAPUZINERWEG 12, STUTTGART Baden-Wurttemberg D-70374, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MORCHER GMBH (Owner Number: 9035333)
Owner / Operator Contact Address
KAPUZINERWEG 12, --, STUTTGART, DE-BW 70374, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P010059

All Registered Proprietary Names

Ring Caliper Capsular Tension Rings

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOC Clip, Iris Retractor Ophthalmic Class 1 886.4350 2000-01-21
HNH Ring, Ophthalmic (Flieringa) Ophthalmic Class 1 886.4350 2006-03-06
MRJ Ring, Endocapsular Unknown Class 3 N/A 2009-07-14

Official Correspondent

Olaf Morcher

US Agent Details

Barbara S. Fant Business: Clinical Research Consultants, Inc. Email: bsfant@crc-regulatory.com Phone: (513) 6073932

Related Public Records

Same Entity

MORCHER GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9617458. Last updated year: 2026. Please use registration number 9617458 when referencing this establishment in official correspondence.
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