CARBOLIFE TECHNOLOGIES GMBH & CO. KG

FDA Device Registration & Listing · Dresden Saxony, DE · Registration 3002847229

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
3002847229
FEI Number
3002847229
Entity Name
CARBOLIFE TECHNOLOGIES GMBH & CO. KG
City/State/Country
Dresden Saxony, DE
Establishment Address
Hermann-Mende-Str. 5-7, Dresden Saxony 01099, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CarboLife technologies GmbH & Co. KG (Owner Number: 10051025)
Owner / Operator Contact Address
Hermann-Mende-Str. 5-7, Dresden, DE-SN 01099, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

QUADRO CURVE GEKKO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNO Accessories, Wheelchair Physical Medicine Class 1 890.3910 2016-01-27

Official Correspondent

Mirko Filler

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

CarboLife technologies GmbH & Co. KG
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 3002847229. Last updated year: 2026. Please use registration number 3002847229 when referencing this establishment in official correspondence.
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