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Sign in to claim this brand3M Deutschland GmbH
US
Last updated May 24, 2026
What 3M Deutschland GmbH makes
The company produces dental materials and tools, including ceramic fabrication materials for dental appliances, silicone and polyether-based impression materials, and dental composites such as glass ionomer cements and resin fillings. It also manufactures single-use cannulas for material injection, mixing nozzles, and hard denture reliners, alongside temporary dental restorative materials like provisional crowns.
These products are authorised as Class I, Class II, or unclassified devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates with a US-based manufacturing presence.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does 3M Deutschland GmbH primarily manufacture?
3M Deutschland GmbH specializes in dental materials and tools. Their portfolio includes ceramic fabrication materials for dental appliances, impression materials like silicone and polyether-based compounds, dental composites such as glass ionomer cements and resin fillings, and single-use cannulas for material injection. They also produce mixing nozzles, hard denture reliners, and temporary restorative materials like provisional crowns.
Where is 3M Deutschland GmbH based, and does it have a manufacturing presence in the US?
While 3M Deutschland GmbH is based in Germany, the company operates with a manufacturing presence in the US. This allows them to produce and distribute their dental devices globally, including those authorised under FDA regulations.
Which regulatory registries list the devices manufactured by 3M Deutschland GmbH?
The devices produced by 3M Deutschland GmbH are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their authorised products, ensuring transparency and compliance with regulatory requirements.
How are the dental devices from 3M Deutschland GmbH classified under FDA regulations?
The dental devices manufactured by 3M Deutschland GmbH are authorised as Class I, Class II, or unclassified (Class U) devices under FDA regulations. The classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety, with Class I being the lowest risk and Class II requiring additional controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- mmm.com
- —
- —
- [email protected]
- Phone
- +1(800)634-2249
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 315731711
Catalogue (1444)
Page 3 of 29| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 3M™ Actisorb™ | 105220 | FDA UDI | U | Active |
| Scotchbond™ Universal Etchant | 41263 | FDA UDI | Class II | Active |
| Lava™ Esthetic | 69337 | FDA UDI | Class II | Active |
| Protemp™ Plus | 46962 | FDA UDI | Class II | Active |
| Lava™ Plus | 69176 | FDA UDI | Class II | Active |
| Sinfony™ | 49670 | FDA UDI | Class II | Active |
| Dimension™ Penta™ H Quick | 36913 | FDA UDI | Class II | Active |
| Sinfony™ | 49490 | FDA UDI | Class II | Active |
| Ketac™ Silver Maxicap™ | 56210 | FDA UDI | Class II | Active |
| Imprint™ 4 Regular | 71519 | FDA UDI | Class II | Active |
| Lava™ Plus | 69227 | FDA UDI | Class II | Active |
| Sinfony™ | 49130 | FDA UDI | Class II | Active |
| Lava™ Plus | 69181 | FDA UDI | Class II | Active |
| RelyX™ Unicem 2 Automix | 56857 | FDA UDI | Class I | Active |
| Ketac™ Universal Aplicap™ | 61098 | FDA UDI | Class II | Active |
| 3m™ | 69947 | FDA UDI | Class II | Active |
| CoJet™ | 68421 | FDA UDI | Class II | Active |
| Sinfony™ | 49480 | FDA UDI | Class II | Active |
| Durelon™ | 38237 | FDA UDI | Class II | Active |
| Imprint™ 4 Heavy | 71492 | FDA UDI | Class II | Active |
| Imprint™ 3 Light Body | 10778 | FDA UDI | Class II | Active |
| RelyX™ Unicem Aplicap™ | 56817 | FDA UDI | Class I | Active |
| Ketac™ Fil Plus Aplicap™ | 55025 | FDA UDI | Class II | Active |
| Imprint™ 4 Super Quick Light | 71490 | FDA UDI | Class II | Active |
| Imprint™ 4 Super Quick Heavy | 71493 | FDA UDI | Class II | Active |
| Lava™ Frame | 68581 | FDA UDI | Class II | Active |
| 3m™ | 71225 | FDA UDI | Class I | Active |
| Photac™ Fil Quick Aplicap™ | 61010 | FDA UDI | Class II | Active |
| Lava™ Frame Shade | 68578 | FDA UDI | Class II | Active |
| Sinfony™ | 49450 | FDA UDI | Class II | Active |
| Sinfony™ | 49320 | FDA UDI | Class II | Active |
| Sinfony™ | 49260 | FDA UDI | Class II | Active |
| Imprint™ 4 Preliminary Super Quick | 71540 | FDA UDI | Class II | Active |
| Lava™ Plus | 69262 | FDA UDI | Class II | Active |
| Permadyne™ Garant™ 2:1 | 30413 | FDA UDI | Class I | Active |
| Imprint™ 4 Penta™ Putty | 71499 | FDA UDI | Class II | Active |
| Sinfony™ | 49870 | FDA UDI | Class II | Active |
| Rocatec™ | 68370 | FDA UDI | Class II | Active |
| 3M™ ESPE™ Impregum™ Penta™ | 31731 | FDA UDI | Class II | Active |
| Lava™ Esthetic | 69341 | FDA UDI | Class II | Active |
| Photac™ Fil Quick Aplicap™ | 61083 | FDA UDI | Class II | Active |
| Photac™ Fil Quick Aplicap™ | 61050 | FDA UDI | Class II | Active |
| Sinfony™ | 49280 | FDA UDI | Class II | Active |
| 3M™ Imprint™ | 71498 | FDA UDI | Class I | Active |
| Lava™ Frame Shade | 68580 | FDA UDI | Class II | Active |
| 3M™ RelyX™ | 56918 | FDA UDI | Class I | Active |
| Dimension™ Penta™ H | 36714 | FDA UDI | Class II | Active |
| Sinfony™ | 49680 | FDA UDI | Class II | Active |
| Sinfony™ | 49220 | FDA UDI | Class II | Active |
| Sinfony™ | 49630 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- 3M Deutschland GmbH Neuss North Rhine-Westphalia · DE FEI 3008512935