BEELINE GMBH

FDA Device Registration & Listing · COLOGNE North Rhine-Westphalia, DE · Registration 3008204044

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
3008204044
FEI Number
3008204044
Entity Name
BEELINE GMBH
City/State/Country
COLOGNE North Rhine-Westphalia, DE
Establishment Address
DILLENBURGER STR 76, COLOGNE North Rhine-Westphalia 51105, DE
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device
Owner / Operator
BEELINE GMBH (Owner Number: 10056620)
Owner / Operator Contact Address
DILLENBURGER STR 76, COLOGNE, DE-NOTA 51105, DE
Initial Importer Flag
N
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
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2017-12-26

Official Correspondent

MARTINA FROMM

US Agent Details

GOEKHAN TAS Business: BEELINE IMPORT AND SERVICES Email: GOEKHAN.TAS@BEELINE-GROUP.COM Phone: (901) 3704008

Related Public Records

Same Entity

BEELINE 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 3008204044. Last updated year: 2026. Please use registration number 3008204044 when referencing this establishment in official correspondence.
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