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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 32 of 70

Device	Model / Reference	Registries	Class	Status
3M™ ESPE™ Iso-Form™	L-61	FDA UDI	Class I	Active
3m™	68960	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-57	FDA UDI	Class I	Active
Steri-Drape™	1031	FDA UDI	Class II	Active
Ketac™	3305A1-S	FDA UDI	Class II	Unknown
3M™ Cavilon™	5051G	FDA UDI	Class I	Active
3M™ Medipore™	3571	FDA UDI	Class I	Active
Bair Hugger™	63700	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-51	FDA UDI	Class I	Active
3M™ Littmann®	5647	FDA UDI	Class I	Active
3M™ Tegaderm™	9132	FDA UDI	U	Active
3M™ Nexcare™	SLT-SIOC	FDA UDI	Class I	Active
3M™ ACE™ Brand	207465	FDA UDI	Class I	Active
3M™ Littmann®	2454	FDA UDI	Class I	Active
Curos™	CM5-200	FDA UDI	U	Active
3M™ Unitek™	900115	FDA UDI	Class I	Active
Bair Hugger™ Novaplus™	40034	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6203	FDA UDI	Class I	Active
RelyX™	7614TR	FDA UDI	Class II	Active
Steri-Drape™	9047	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6206	FDA UDI	Class I	Active
3M™ Unitek™	907032	FDA UDI	Class I	Active
Filtek™	6032A3.5	FDA UDI	Class II	Active
3M™ Transpore™	1527S-2	FDA UDI	Class I	Active
Attest™	1262P	FDA UDI	Class II	Active
3M™ Littmann®	8490	FDA UDI	Class II	Active
Clinpro™	12626	FDA UDI	Class II	Active
3M™ Micropore™	2770-1	FDA UDI	Class I	Active
3m™	40068	FDA UDI	Class II	Active
3M™ Tegaderm™	90602	FDA UDI	Class I	Active
Bair Hugger™	44068	FDA UDI	Class II	Active
Bair Hugger™	90131	FDA UDI	Class II	Unknown
Ranger™	24355	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2124	FDA UDI	Class I	Active
E-A-Rlink™	420-2007	FDA UDI	Class I	Active
3m™ Espe™	13	FDA UDI	Class I	Active
3M™ Medipore™	2860S-4U	FDA UDI	Class I	Active
3M™ Littmann® Classic II™	2157	FDA UDI	Class I	Active
Lava™	1314B1-LT	FDA UDI	Class II	Active
Filtek™	6029A3B	FDA UDI	Class II	Active
Filtek™	6032A3	FDA UDI	Class II	Active
Red Dot™	2660-5	FDA UDI	Class II	Active
3m™	801203	FDA UDI	Class I	Active
3m™	8180F	FDA UDI	Class II	Active
Paradigm™	1480C2	FDA UDI	Class II	Active
Paradigm™	5311	FDA UDI	Class II	Active
Steri-Drape™	9088	FDA UDI	Class II	Active
Filtek™	4720C2	FDA UDI	Class II	Active
3M™ Unitek™	900316	FDA UDI	Class I	Active
Fast Release Varnish	12157S	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.