3M DEUTSCHLAND GMBH

FDA Device Registration & Listing · KAMEN North Rhine-Westphalia, DE · Registration 3004083376

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
3004083376
FEI Number
3004083376
Entity Name
3M DEUTSCHLAND GMBH
City/State/Country
KAMEN North Rhine-Westphalia, DE
Establishment Address
Plant Kamen, EDISONSTRASSE 6, KAMEN North Rhine-Westphalia 59174, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
3M COMPANY (Owner Number: 2110898)
Owner / Operator Contact Address
2510 Conway Avenue, Saint Paul, MN 55144, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BANDAGE, ELASTIC 3M Tape and bandage, adhesive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQM Bandage, Elastic General Hospital Class 1 880.5075 2003-06-05
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2003-08-21

Official Correspondent

No official correspondent registered.

US Agent Details

Jeffery Schorr Business: 3M Center Email: jjschorr@solventum.com Phone: (210) 2556721

Related Public Records

Same Entity

3M COMPANY
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005088750 3M POLAND MANUFACTURING SP. Z O.O WROCLAW Dolnoslaskie, PL
3006580861 3M Japan Products Limited Higashine-shi Yamagata, JP
1929938 3M COMPANY Valley, NE, US
2122594 3M COMPANY Hutchinson, MN, US
1717046 3M COMPANY BROOKINGS, SD, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004083376. Last updated year: 2026. Please use registration number 3004083376 when referencing this establishment in official correspondence.
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