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Sign in to claim this brandCMP INDUSTRIES LLC
US
Last updated May 23, 2026
What CMP INDUSTRIES LLC makes
CMP Industries LLC manufactures dental materials for prosthetic fabrication, including resin artificial teeth, dental casting alloys, and thermoplastic/resin materials for appliance construction. Their portfolio also includes bite registration rims, which aid in creating accurate dental impressions for custom appliances.
The company’s devices are regulated under FDA’s Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 types of medical devices does CMP Industries LLC manufacture?
CMP Industries LLC specializes in dental materials used for prosthetic fabrication. Their portfolio includes resin artificial teeth, dental casting non-noble alloys, thermoplastic and resin materials for dental appliance fabrication, and bite registration rims. These products support the creation of custom dental appliances and restorations, such as crowns, bridges, and orthodontic devices.
Where is CMP Industries LLC based, and what does that mean for their regulatory oversight?
CMP Industries LLC is based in the United States, meaning their devices fall under FDA jurisdiction. The FDA regulates these products through classifications like Class I (generally low-risk) and Class II (moderate-risk), requiring compliance with relevant guidelines to ensure safety and effectiveness in dental applications.
Are CMP Industries LLC’s devices listed in any regulatory registries, and why does that matter?
Yes, CMP Industries LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify specific devices in the market, ensuring transparency for healthcare providers, regulators, and patients. Listing in the UDI system aids in recall management, post-market surveillance, and compliance verification.
How are CMP Industries LLC’s dental devices classified by the FDA, and what does that classification indicate?
CMP Industries LLC’s devices are classified under FDA’s Class I and Class II categories. Class I typically covers low-risk items like some dental materials that pose minimal harm if used as intended, while Class II includes moderate-risk devices requiring special controls (e.g., performance standards or post-market surveillance) to mitigate potential risks. Classification determines regulatory requirements for manufacturing, labeling, and compliance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 002064319
Catalogue (2123)
Page 37 of 43| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Massad | MALC1L4 | FDA UDI | Class II | Active |
| Massad | MPUA00I34U | FDA UDI | Class II | Active |
| Nobilium | NAUC2S3 | FDA UDI | Class II | Active |
| Massad | MPUC2I34U | FDA UDI | Class II | Active |
| Nobilium | NAUB1S3 | FDA UDI | Class II | Active |
| Nobilium | 8134N | FDA UDI | Class II | Active |
| Nobilium | NAUC2O5 | FDA UDI | Class II | Active |
| Massad | MAUC3S1 | FDA UDI | Class II | Active |
| Nobilium | NALA35L14 | FDA UDI | Class II | Active |
| Massad | MAUC2P4 | FDA UDI | Class II | Active |
| Massad | MAUB1K3 | FDA UDI | Class II | Active |
| Nobilium | 689226R | FDA UDI | Class I | Active |
| Nobilium | 689LT4U100 | FDA UDI | Class I | Active |
| Nobilium | NPLD430L | FDA UDI | Class II | Active |
| Nobilium | 3747 | FDA UDI | Class II | Active |
| Nobilium | NAUD2T6 | FDA UDI | Class II | Active |
| Nobilium | NALD3L7 | FDA UDI | Class II | Active |
| Massad | MALA0Z2 | FDA UDI | Class II | Active |
| Massad | MAUC4T1 | FDA UDI | Class II | Active |
| Nobilium | NAUA4O8 | FDA UDI | Class II | Active |
| Nobilium | NPLB232L | FDA UDI | Class II | Active |
| Massad | MAUA3IO2 | FDA UDI | Class II | Active |
| Nobilium | NPLA134L | FDA UDI | Class II | Active |
| Nobilium | 8105 | FDA UDI | Class II | Active |
| Nobilium | 804009K | FDA UDI | Class II | Active |
| Nobilium | EQC6 | FDA UDI | Class II | Active |
| Nobilium | 0129-25 | FDA UDI | Class II | Active |
| Nobilium | 3306 | FDA UDI | Class II | Active |
| Massad | MAUA1O1 | FDA UDI | Class II | Active |
| Nobilium | NAUD4S5 | FDA UDI | Class II | Active |
| Nobilium | 804003 | FDA UDI | Class II | Active |
| Nobilium | NAUC4T9 | FDA UDI | Class II | Active |
| Nobilium | 10015S | FDA UDI | Class II | Active |
| Nobilium | NPLB234L | FDA UDI | Class II | Active |
| Nobilium | NPLC232L | FDA UDI | Class II | Active |
| Nobilium | NPLD230L | FDA UDI | Class II | Active |
| Massad | MPLD334L | FDA UDI | Class II | Active |
| Nobilium | NALC2L5 | FDA UDI | Class II | Active |
| Nobilium | NAUB4S4 | FDA UDI | Class II | Active |
| Massad | MAUD4S3 | FDA UDI | Class II | Active |
| Nobilium | 81102 | FDA UDI | Class II | Active |
| Nobilium | NAUD3T5 | FDA UDI | Class II | Active |
| Massad | MAUA3T8 | FDA UDI | Class II | Active |
| Massad | MALA2IL1 | FDA UDI | Class II | Active |
| Massad | MAUD2T5 | FDA UDI | Class II | Active |
| Nobilium | NAUB4O8 | FDA UDI | Class II | Active |
| Nobilium | EDENTB900 | FDA UDI | Class I | Active |
| Nobilium | NPUC334U | FDA UDI | Class II | Active |
| Nobilium | 689622-12 | FDA UDI | Class I | Active |
| Nobilium | 687432-12 | FDA UDI | Class I | 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 Recalls (6)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
CMP Industries LLC has six recall records initiated between November 18, 2013, and September 12, 2018, all of which are marked as terminated. The reasons cited include potential rust in Impak Acrylic Liquid Batch 103113, with one instance specifically noting the absence of notification to the district during the recall process, as well as general occurrences of foreign material in the product.
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 |
|---|---|---|---|---|
| Sep 12, 2018 | Z-0292-2019 | — | terminated | Foreign material in product |
| Sep 12, 2018 | Z-0293-2019 | — | terminated | Foreign material in product |
| Apr 28, 2016 | Z-2097-2016 | — | terminated | Possible presence of foreign material (rust). |
| Apr 28, 2016 | Z-2098-2016 | — | terminated | Possible presence of foreign material (rust). |
| Mar 2, 2016 | Z-2089-2016 | — | terminated | Possible presence of foreign material (rust). |
| Nov 18, 2013 | Z-1089-2016 | — | terminated | During the current inspection of CMP Industries, the FDA Investigator discovered that the firm had conducted a recall of Impak Acrylic Liquid Batch 103113 in 2013 due to potential rust without notifying the district. |