Data / Medical devices / Israel / Global Dental Transfer Ltd
Global Dental Transfer Ltd: FDA-registered device maker in Beer Sheva Southern, Israel, 2 510(k) clearances
Global Dental Transfer Ltd is registered with the FDA (registration 3017013344) in Beer Sheva Southern, Israel. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 21, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017013344
- Address
- Yitzhak Ben Zvi 9/64, Beer Sheva Southern, Israel, 8489327
- Owner or operator
- Global Dental Transfer Ltd (10074916)
- Roles
- Repackager or relabeler
- First device listed
- June 2, 2020
- Registered through
- 2026
- Brand names listed
- Global Dental Transfer Dental Implant System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Repackager or relabeler | accessdata.fda.gov |
| Non-Irrigation Endosseous Dental Implant Drill Bits | QRQ | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| April 21, 2025 | K250176 | DAND Dental Implant System | DZE | Substantially Equivalent | D.A.N.D. Metal Industries North, Ltd. | accessdata.fda.gov |
| April 1, 2020 | K200188 | DSI Dental Implant System | DZE | Substantially Equivalent | Dsi Dental Solutions, 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
- All makers of Non-Irrigation Endosseous Dental Implant Drill Bits
Updated April 21, 2025. 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.