ROEDER DENTALINSTRUMENTE GMBH & CO. KG

FDA Device Registration & Listing · Munich Bavaria, DE · Registration 3003386548

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
3003386548
FEI Number
3003386548
Entity Name
ROEDER DENTALINSTRUMENTE GMBH & CO. KG
City/State/Country
Munich Bavaria, DE
Establishment Address
Bahnhofstr. 37, Neufahrn, Munich Bavaria 85375, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Roeder Dentalinstrumente GmbH & Co. KG (Owner Number: 10082190)
Owner / Operator Contact Address
Bahnhofstr. 37, Neufahrn, Munich, DE-BY 85375, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Optima Mouth Mirrors EC-Aktiv HR-Front Cheek Retraction Mirror Clarima

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAX Mirror, Mouth Dental Class 1 872.4565 2021-06-24

Official Correspondent

Mindy McCann

US Agent Details

Mindy McCann Business: Qserve Group US Inc. Email: usagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Roeder Dentalinstrumente GmbH & Co. KG
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 3003386548. Last updated year: 2026. Please use registration number 3003386548 when referencing this establishment in official correspondence.
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