Registered with FDA
Common Sense Dental Products
Spring Lake, MI, United States. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 37 registrations outside the US
- Establishments
- 1United States
Registered in 3 markets
Where regulators' registries name Common Sense Dental Products as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Lister | Common Sense Dental Products | 4 device types | — | Below |
| United Kingdom | MHRA | Manufacturer | Common Sense Dental Products | 4 | — | Pure Global AI |
| European Union | EUDAMED | Manufacturer | Common Sense Dental Products | 3 | — | 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
Devices listed with FDA
What Common Sense Dental Products currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Articulation PaperEFH · Class 1 | — | Lister | Prep Check | 2005 |
| Dental Retractor AccessoriesEIF · Class 1 | Dental hand instruments | Lister | LogiBloc | 2013 |
| Dental Instrument HandleEJB · Class 1 | Dental hand instruments | Lister | FlexiWedgeFlexiWedge Curve | 1999 |
| Endodontic Pulp Canal FileEKS · Class 1 | Endodontic files | Lister | EndoPoint | 2012 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| COMMON SENSE DENTAL PRODUCTSFDA reg. 1836229 | Spring Lake, MI, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9038910). 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.