Not currently registered with FDA under this name
Ditron Precision, Ltd.
Netanya, Israel. Named as applicant on 2 dental 510(k) clearances between 2014 and 2016. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22014–2016
- Markets registered in
- 24 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2007–2026
Registered in 2 markets
Where regulators' registries name Ditron Precision, Ltd. 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 | Ditron Precision, Ltd. | 2 clearances | 2014–2016 | Below |
| Israel | AMAR | Registration holder | DITRON PRECISION LTD.DITRON PRECISION LTD | 4 | — | 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 Ditron Precision, Ltd. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 28 Oct 2016 | K161497 | Dental Implants and Abutments | DZE Root-Form Endosseous Implant |
| 17 Oct 2014 | K140728 | MPI - MOLECULAR PRECISION IMPLANT, CPI - CYLINDRICAL PRECISION IMPLANT, OPI - ONE PIECE IMPLANT, DENTAL ABUTMENTS AND PR | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Ditron Dental Ltd (2).
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.