Not currently registered with FDA under this name
Cmp Industries, LLC
Albany, NY, United States. Named as applicant on 6 dental 510(k) clearances between 1990 and 2017. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 61990–2017
- Markets registered in
- 464 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1990–2026
Registered in 4 markets
Where regulators' registries name Cmp Industries, LLC as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Cmp Industries, LLC | 6 clearances | 1990–2017 | Below |
| Canada | Health Canada | Registration holder | CMP INDUSTRIES LLC | 32 | 2002–2014 | Pure Global AI |
| South Korea | MFDS | Manufacturer | CMP Industries LLCCMP Industries,Inc. · CMP Industries, Inc. · +2 | 24 | 1998–2012 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | CMP INDUSTRIES LLC. | 8 | 2015–2017 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Cmp Industries, LLC as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 2 Oct 2017 | K170375 | Nobilplast Denture Resin | EBI Rebasing Repairing Relining Denture Resin |
| 20 Feb 2008 | K072851 | POLYSTAR 79 DENTURE BASE RESIN | EBI Rebasing Repairing Relining Denture Resin |
| 19 Oct 2007 | K072402 | FLEX-STAR V | EBI Rebasing Repairing Relining Denture Resin |
| 19 Dec 2003 | K033020 | IMPAK ACRYLIC REPAIR RESIN LIQUID | EBI Rebasing Repairing Relining Denture Resin |
| 5 Sep 1995 | K953594 | VULCAN | EJH Base Metal Alloy |
| 4 Oct 1990 | K902972 | FLEXOR (DENTURE ACRYLIC RELINE MATERIAL) | EBI Rebasing Repairing Relining Denture Resin |
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.