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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 40 of 70

Device	Model / Reference	Registries	Class	Status
Attest™	1264P	FDA UDI	Class II	Active
3m™	9680	FDA UDI	Class I	Active
3M™ Tegaderm™	90648	FDA UDI	Class I	Active
3M™ Tegaderm™	1680	FDA UDI	Class I	Active
3M™ Littmann®	2175	FDA UDI	Class I	Active
Lava™	5072B1-HT	FDA UDI	Class II	Active
Bair Hugger™	37000	FDA UDI	Class II	Active
3M™ Unitek™	900321	FDA UDI	Class I	Active
Bair Hugger™	11101	FDA UDI	Class II	Active
Steri-Drape™	9072	FDA UDI	Class II	Active
Filtek™	6020B2	FDA UDI	Class II	Active
3M™ Unitek™	900136	FDA UDI	Class I	Active
3M™ Transpore™	1527-154	FDA UDI	Class I	Active
3m™	3303DT	FDA UDI	Class II	Active
3M™ Nexcare™	771-1PK	FDA UDI	Class I	Active
Steri-Drape™	9045R	FDA UDI	Class II	Active
3M™ Nexcare™	771-2PK	FDA UDI	Class I	Active
Red Dot™	2235	FDA UDI	Class II	Active
3M™ Tegaderm™	90021	FDA UDI	Class I	Active
3M™ ESPE™ MDI O-Ball Prosthetic Head	1.8 mm x 15 mm	FDA UDI	Class II	Unknown
Lava™	2914A1-LT	FDA UDI	Class II	Active
3M™ Filtek™	6032B1	FDA UDI	Class II	Active
Bair Hugger™ Novaplus™	44034	FDA UDI	Class II	Active
3M™ Nexcare™	782	FDA UDI	Class I	Active
3m™	SPS-YA1100	FDA UDI	Class I	Active
Steri-Drape™	9012LA	FDA UDI	Class II	Active
Steri-Drape™	9023	FDA UDI	Class II	Active
Littmann®	3200BU	FDA UDI	Class II	Active
3M™ Cavilon™	5050	FDA UDI	Class I	Active
3m™	1860S	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5871	FDA UDI	Class I	Active
3M™ ESPE™ MDI Max with O-Ball Head and Collar	2.4 mm x 18 mm	FDA UDI	Class II	Unknown
Steri-Drape™	9100	FDA UDI	Class II	Active
3M™ Medipore™	3570	FDA UDI	Class I	Active
Espe™	2042FP	FDA UDI	Class II	Unknown
3M™ Cavilon™	5050	FDA UDI	Class I	Active
3M™ Littmann®	6163	FDA UDI	Class I	Active
Concise™	1930	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6162	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5621	FDA UDI	Class I	Active
Lava™	2614B1-LT	FDA UDI	Class II	Active
3M™ Unitek™	900509	FDA UDI	Class I	Active
3M™ Unitek™	900445	FDA UDI	Class I	Active
Vanish™ XT	12158	FDA UDI	Class II	Active
3m™	800417	FDA UDI	Class I	Active
3m™ Espe™	102	FDA UDI	Class I	Active
3M™ Durapore™	1590S-1	FDA UDI	Class I	Active
3M™ Red Dot™	2560-3	FDA UDI	Class II	Active
Attest™	41482V	FDA UDI	Class II	Active
3M™ Scotchcast™	WDP6	FDA UDI	Class I	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.