Not currently registered with FDA under this name
Inter-Med/Vista Dental Products
Racine, WI, United States. Named as applicant on 2 dental 510(k) clearances between 2017 and 2020. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22017–2020
- Markets registered in
- 29 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2007–2026
Registered in 2 markets
Where regulators' registries name Inter-Med/Vista 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 | Applicant | Inter-Med/Vista Dental Products | 2 clearances | 2017–2020 | Below |
| Taiwan | TFDA | Manufacturer | INTER-MED/VISTA DENTAL PRODUCTS | 9 | 2015–2026 | 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 Inter-Med/Vista Dental Products as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 11 Mar 2020 | K193447 | Vista Dyes | LFC Caries Detection Device |
| 8 Jun 2017 | K170101 | Valiant Curing Light | EBZ Ultraviolet Activator for Polymerization |
Some of these clearances are listed with FDA today by another company: Inter-Med, Inc. (1).
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.