3M COMPANY

FDA Device Registration & Listing · Saint Paul, MN, US · Registration 2110898

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
2110898
FEI Number
2110898
Entity Name
3M COMPANY
City/State/Country
Saint Paul, MN, US
Establishment Address
2510 Conway Ave., Saint Paul, MN 55144, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
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
PMA Number
N/A

All Registered Proprietary Names

Futuro Anti-Embolism Stockings Dressing, wound, occlusive Splint, Clavicle ORTHOSIS, TRUNCAL/ORTHOSIS, LIMB 3M 3M STOMASEAL ADHESIVE DIS 3M 3M 3M Respirator Nexcare Basal Digital Thermometer Futuro Compression Hosiery JOINT, KNEE, EXTERNAL BRACE 3M BANDAGE, ELASTIC SUPPORT, ARM 3M 3M Pack, hot or cold, reusable Orthosis, cervical 3M™ ORTHOSIS, LIMB BRACE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) General Hospital Class 2 880.5780 2013-03-12
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2025-12-16
IQJ Splint, Clavicle Physical Medicine Class 1 890.3490 2026-01-12
MRI Orthosis, Truncal/Orthosis, Limb Physical Medicine Class 1 890.3490 2009-07-31
EZS Appliance, Colostomy, Disposable Gastroenterology, Urology Class 1 876.5900 1996-04-08
NEC Bandage, Liquid, Skin Protectant General Hospital Class 1 880.5090 2004-11-08
NZJ Respirator, N95, For Use By The General Public In Public Health Medical Emergencies General Hospital Class 2 880.6260 2007-12-28
LHD Device, Fertility Diagnostic, Proceptive Unknown Class U N/A 2013-03-12
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2007-12-06
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) General Hospital Class 2 880.5780 2013-03-12
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 1992-12-15
ILI Sling, Arm Physical Medicine Class 1 890.3640 2009-02-16
FQM Bandage, Elastic General Hospital Class 1 880.5075 2003-06-05
IOY Support, Arm Physical Medicine Class 1 890.3475 2009-02-16
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2009-02-16
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 1997-02-20
IQK Orthosis, Cervical Physical Medicine Class 1 890.3490 2009-02-16
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 1995-06-02
MSH Respirator, 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
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
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31
K201622 Guangdong Kingfa Sci. & Tech.Co., Ltd. Medical surgical mask 2020-11-24
K881618 3M Company ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK 1988-05-09
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0022-2013 3M Company Health Care Business 3M Center 2
3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed to sterilize heat- and/or moisture-sensitive devices. This gas sterilizer/aerator is intended for indoor use only.
Z-0027-2007 N/A 2
3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.
Z-0037-05 N/A 2
NOVAPLUS Electrosurgical Grounding Pads, Split with Cord Catalog No. 7179V
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2110898. Last updated year: 2026. Please use registration number 2110898 when referencing this establishment in official correspondence.
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