Data / Medical devices / Israel / RDJ Tov Implant Ltd
RDJ Tov Implant Ltd: FDA-registered device maker in Jerusalem, Israel, 1 510(k) clearance
RDJ Tov Implant Ltd is registered with the FDA (registration 3033524692) in Jerusalem, Israel. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 15, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033524692
- Address
- Mutsafi Street 8 4 View Tower, Jerusalem, Israel, 96420
- Owner or operator
- RDJ TOV Implant Ltd (10091707)
- Roles
- Specification developer
- First device listed
- October 25, 2024
- Registered through
- 2026
- Brand names listed
- TOV Dental Implant System, TOV Dental Implant System Tools and Accessories
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Specification developer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Specification developer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 15, 2024 | K240837 | TOV Dental Implant System | DZE | Substantially Equivalent | Rdj Tov Implant, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Accessories, Implant, Dental, Endosseous
Updated August 15, 2024. 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.