Data / Medical devices / Drill, Dental, Intraoral / Israel
FDA-registered makers of Drill, Dental, Intraoral in Israel: 11 establishments
11 establishments in Israel are registered with the FDA to make Drill, Dental, Intraoral (product code DZA). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Drill, Dental, Intraoral
- Product code
- DZA
- Country
- Israel
Makers of Drill, Dental, Intraoral in Israel
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| A.B. Dental Devices Ltd | Ashdod Southern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cortex Dental Implants Industries Ltd. | Shlomi Northern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentin Implants Technologies Ltd. | Mizpe Aviv Northern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iq Implants Ltd | Omer Southern, Israel | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Khoury Dent Ltd Via Kasko K.N Ltd | Karmiel Northern, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Noga Medical Products Ltd. | SHLOMI Northern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Noris Medical Ltd. | Nesher Haifa, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nova Implants Ltd | Or-Yehuda Tel Aviv, Israel | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paltop Advanced Dental Solutions Ltd | Caesarea Central, Israel | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| T.A.G. Medical Products Corporation Ltd | GAATON Northern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Uniqa Dental Ltd | Netanya Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.