Manufacturer registered with FDA
Euroteknika
SALLANCHES, France. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 2
- Brands and models
- 2
- 510(k) clearances
- 12025–2025
- Markets registered in
- 460 registrations outside the US
- Establishments
- 1France
510(k) clearances per year, 2007–2026
Registered in 4 markets
Where regulators' registries name Euroteknika as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Euroteknika | 1 clearances | 2025–2025 | Below |
| Colombia | INVIMA | Manufacturer | EUROTEKNIKA | 28 | — | Pure Global AI |
| European Union | EUDAMED | Registration holder | EUROTEKNIKA | 24 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | EUROTEKNIKA | 8 | 2011–2016 | 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 Euroteknika currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | iPhysio System Try-in Abutments | 2025 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | iPhysio System Profile Designer, iPhysio System Temporary Abutments | 2025 |
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 |
|---|---|---|
| EUROTEKNIKAFDA reg. 3007521935 | SALLANCHES Haute-Savoie, France | Complaint file establishment, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10030222). 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.