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3M COMPANY

United States·US-MF-000014086

Last updated September 17, 2026

What 3M COMPANY makes

3M COMPANY manufactures a range of medical devices including preformed dental crowns, dental composite resins, mechanical external stethoscopes, patient surgical drapes, hypoallergenic skin adhesive tapes, exudate-absorbent dressings, external circulating-air core temperature regulation system pads, and resin dental inlays. They also produce orthopedic supports such as the FUTURO™ Wraparound Ankle Support, FUTURO™ Night Wrist Support, and FUTURO™ Comfort Elbow Support with Pressure Pads.

The company's portfolio includes Class I, Class II, and U devices, which are listed in the EUDAMED and FDA UDI registries. 3M COMPANY is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does 3M COMPANY manufacture?

3M COMPANY produces a variety of medical devices including preformed dental crowns, dental composite resins, mechanical external stethoscopes, patient surgical drapes, hypoallergenic skin adhesive tapes, exudate-absorbent dressings, temperature regulation pads, and resin dental inlays. They also manufacture orthopedic supports like the FUTURO™ Wraparound Ankle Support and FUTURO™ Night Wrist Support.

Where is 3M COMPANY based?

3M COMPANY is based in the United States. The company operates from its headquarters located in the US, where it designs, manufactures, and distributes its medical devices to various markets.

Which regulatory registries list 3M COMPANY's devices?

3M COMPANY's medical devices are listed in the EUDAMED and FDA UDI registries. These databases track medical devices to ensure proper identification, tracking, and regulation throughout their lifecycle in the respective markets.

How are 3M COMPANY's devices classified?

3M COMPANY's medical devices are classified as Class I, Class II, and U devices. Class I devices pose the lowest risk, Class II devices require more regulatory controls, and U devices are unclassified. This classification determines the level of regulatory oversight each product receives.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: 2510, Conway Avenue, St.Paul, United States
Website: solventum.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)634-2249
PRRC Contact: Harry Janiski
EUDAMED SRN: US-MF-000014086
FDA FEI Number: 2110898
DUNS Number: 830016148

Catalogue (3490)

Page 36 of 70

Device	Model / Reference	Registries	Class	Status
Steri-Drape™	9067	FDA UDI	Class II	Active
Lava™	2912A3.5-LT	FDA UDI	Class II	Active
3m™ Espe™	42	FDA UDI	Class I	Active
3M™ Nexcare™	W3590	FDA UDI	Class I	Active
3M™ Transpore™	1527-224	FDA UDI	Class I	Active
3M™ Littmann®	2451	FDA UDI	Class I	Active
3m™ Espe™	940444	FDA UDI	Class I	Active
Vanish™	12149M	FDA UDI	Class II	Active
3M™ Unitek™	900242	FDA UDI	Class I	Active
3M™ Red Dot™	2560-3	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5633	FDA UDI	Class I	Active
Steri-Drape™	1060	FDA UDI	Class II	Active
Steri-Drape™	9086	FDA UDI	Class II	Active
3m™	44068	FDA UDI	Class II	Active
Futuro™	71072EN	FDA UDI	Class II	Active
3M™ Medipore™	3568	FDA UDI	Class I	Active
Aura™	1870+	FDA UDI	Class II	Active
3M™ Littmann®	8838	FDA UDI	Class II	Active
3M™ Tegaderm™	1674	FDA UDI	Class I	Active
Tegaderm™	90301	FDA UDI	U	Active
3m™ Espe™	914024	FDA UDI	Class I	Active
Steri-Drape™	6678	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-70	FDA UDI	Class I	Active
Vitrebond™	7572	FDA UDI	Class II	Active
3M™ Littmann® Master Classic II™	2632	FDA UDI	Class I	Active
3M™ Unitek™	900211	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2159	FDA UDI	Class I	Active
3M™ Tegaderm™	1620	FDA UDI	Class I	Active
Ranger™	24250	FDA UDI	Class II	Unknown
Bair Hugger™	30000	FDA UDI	Class II	Active
3M™ Steri-Strip™	E4542	FDA UDI	Class I	Active
Bair Hugger™	42268	FDA UDI	Class II	Active
3m™ Espe™	940536	FDA UDI	Class I	Active
3m™ Espe™	6UR3	FDA UDI	Class I	Active
3M™ Unitek™	907056	FDA UDI	Class I	Active
3M™ Tegaderm™	1634	FDA UDI	Class I	Active
3M™ Unitek™ Temporary Anchorage Device (TAD)	8 mm	FDA UDI	Class II	Active
3M™ Filtek™	749-300	FDA UDI	Class I	Active
3M™ Medipore™	2866S	FDA UDI	Class I	Active
3M™ Durapore™	1538-3D	FDA UDI	Class I	Active
Bair Hugger™	52301	FDA UDI	Class II	Active
Espe™	1322C	FDA UDI	Class II	Unknown
Futuro™	71068EN	FDA UDI	Class II	Active
3M™ Transpore™	1527-636	FDA UDI	Class I	Active
3m™	1835FS	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6156	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5872	FDA UDI	Class I	Active
3M™ Cavilon™	3346E	FDA UDI	Class I	Active
3M™ Attest™	41360	FDA UDI	Class II	Active
3M™ Filtek™	6032XW	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

3M Deutschland GmbH (Medical) DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

The 3M Company has 2 recall records, with the earliest initiated on 2025-04-10 and the most recent on 2025-04-22. The statuses recorded are open and classified. The reasons given for the recalls are: a notice was issued to clarify flow rates related to the inlet fluid temperature, and a field action to clarify flow rates and inlet fluid temperatures along with the location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Apr 22, 2025	Z-2231-2025	—	open, classified	Notice was issued to clarify flow rates related to the inlet fluid temperature.
Apr 10, 2025	Z-2483-2025	—	open, classified	Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.