3M COMPANY

FDA Device Registration & Listing · Valley, NE, US · Registration 1929938

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
1929938
FEI Number
1929938
Entity Name
3M COMPANY
City/State/Country
Valley, NE, US
Establishment Address
600 EAST MEIGS ST., Valley, NE 68064, US
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
K955382
PMA Number
N/A

All Registered Proprietary Names

Electrosurgical, cutting & coagulation & accessories Electrosurgical, cutting & coagulation & accessories

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2026-03-26
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2026-03-26
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2007-12-06

Official Correspondent

DARLA ELGIN

US Agent Details

No US Agent registered (Local establishment).

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
2122594 3M COMPANY Hutchinson, MN, US
1717046 3M COMPANY BROOKINGS, SD, US
3008512935 3M Deutschland GmbH Neuss North Rhine-Westphalia, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

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3012940012 Sutter Medical Technologies USA Inc. Alpharetta, GA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1929938. Last updated year: 2026. Please use registration number 1929938 when referencing this establishment in official correspondence.
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