KOB GmbH

FDA Device Registration & Listing · Wolfstein Rhineland-Palatinate, DE · Registration 8010200

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
8010200
FEI Number
3007858639
Entity Name
KOB GmbH
City/State/Country
Wolfstein Rhineland-Palatinate, DE
Establishment Address
LAUTERSTR. 50, Wolfstein Rhineland-Palatinate 67752, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
KOB GmbH (Owner Number: 8010200)
Owner / Operator Contact Address
Lauterstr. 50, --, Wolfstein, DE-RP 67752, 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
FQM Bandage, Elastic General Hospital Class 1 880.5075 1978-02-14

Official Correspondent

Simone Viering

US Agent Details

Diane Marsilio Business: HARTMANN USA Email: diane.marsilio@hartmann.info Phone: (803) 9851120

Related Public Records

Same Entity

KOB GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008485313 KOB Medical Textiles Pvt. Ltd. Palladam Tamil Nadu, IN

Similar Registrations

Registration Number Establishment Name Location
3005423373 TRI-FI KNITTING, LLC Dunlap, TN, US
3008973900 SAFECARE MEDICAL PRODUCTS CO., LTD. (HEFEI) HEFEI Anhui, CN
3005360866 QEL DOMINICANA S.A. ESPERANZA Valverde, DO
3015414796 COMPRESS INNOVATIONS, LLC Manhasset, NY, US
3004651767 CLEARPOINT MEDICAL Lachine Quebec, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010200. Last updated year: 2026. Please use registration number 8010200 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.