Cmp Industries LLC
United StatesFDA applicant, unverified
Cmp Industries LLC is a medical device manufacturer, with 2,123 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) and 6 FDA recalls as of 15 Nov 2026.
- Devices
- 2,123
- FDA recalls
- 6
Registry facts
- Registries
- FDA GUDID 2,116
- FDA 510(k) 7
- Device classes
- FDA Class II 2,031
- FDA Class I 92
- FDA recalls
- Identifiers
- DUNS 002064319
At a glance
Market reach
- United States
- FDA recalls
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.
Catalogue
Search and filter all 2,123 devicesShowing 1-50 of 2,123
Company details
- DUNS number
- 002064319
FDA recalls
FDA recall records list 6 recalls initiated by CMP INDUSTRIES LLC, the earliest on 2013-11-18 and the most recent on 2018-09-12. By recorded status: 6 terminated. The reasons filed fall into these groups: sterility or contamination and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 2
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2018
- 12 Sep 2018 Z-0292-2019 Class II Terminated Foreign material in product
Full distribution text
- 12 Sep 2018 Z-0293-2019 Class II Terminated Foreign material in product
Full distribution text
- 12 Sep 2018 Z-0292-2019 Class II Terminated Foreign material in product
2016
- 28 Apr 2016 Z-2097-2016 Class II Terminated Possible presence of foreign material (rust).
- 28 Apr 2016 Z-2098-2016 Class II Terminated Possible presence of foreign material (rust).
- 2 Mar 2016 Z-2089-2016 Class II Terminated Possible presence of foreign material (rust).
2013
- 18 Nov 2013 Z-1089-2016 Class II 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.
Frequently asked questions
How many devices does CMP INDUSTRIES LLC have in the registry?
The registry currently lists 2123 devices for CMP INDUSTRIES LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list CMP INDUSTRIES LLC's devices?
Among its 50 most recently registered devices, CMP INDUSTRIES LLC has devices listed in FDA GUDID (50 devices).
What risk classes do CMP INDUSTRIES LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for CMP INDUSTRIES LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for CMP INDUSTRIES LLC?
FDA recall records list 6 recalls initiated by CMP INDUSTRIES LLC, the most recent initiated on 12 Sep 2018. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from CMP INDUSTRIES LLC in the registry?
The most recently registered devices listed for CMP INDUSTRIES LLC include MASSAD MPUD2I36U, NOBILIUM 21142, NOBILIUM NPUA3530U and MASSAD MAUD2IO4.