ONCARE GmbH

FDA Device Registration & Listing · Munich Bavaria, DE · Registration 3023709806

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
3023709806
FEI Number
3023709806
Entity Name
ONCARE GmbH
City/State/Country
Munich Bavaria, DE
Establishment Address
Balanstr. 71a, Munich Bavaria 81541, DE
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
ONCARE GmbH (Owner Number: 10085839)
Owner / Operator Contact Address
Balanstr. 71a, Munich, DE-BY 81541, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

myoncare

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2022-08-19

Official Correspondent

Horst Joachim Mayer

US Agent Details

Doug Dockhorn Business: Veranex Inc. Email: usagent@veranex.com Phone: (919) 8276653

Related Public Records

Same Entity

ONCARE GmbH
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 3023709806. Last updated year: 2026. Please use registration number 3023709806 when referencing this establishment in official correspondence.
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