Data / Medical devices / Israel / Dentin Implants Technologies Ltd.
Dentin Implants Technologies Ltd.: FDA-registered device maker in Mizpe Aviv Northern, Israel, 1 510(k) clearance
Dentin Implants Technologies Ltd. is registered with the FDA (registration 3009737865) in Mizpe Aviv Northern, Israel. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 5, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009737865
- Address
- Mizpe Aviv Industrial Park 142, Mizpe Aviv Northern, Israel, 20187
- Owner or operator
- DENTIN Implants Technologies Ltd. (10041411)
- Roles
- Manufacturer, Specification developer
- First device listed
- July 20, 2012
- Registered through
- 2026
- Brand names listed
- Abutment System, Aesthetic Minor Unit, Anatomic Angulated Titanium Abutment, Anatomic Titanium Abutment, Angular Curve, Angular Curve Narrow Three, Angular multi unit, Angular smooth and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Bur, Dental | EJL | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| July 5, 2012 | K120530 | DENTIN DENTAL IMPLANTS SYSTEM: RAPID, CLASSIC, PRESTIGE, ONE PIECE, DENTIN DENTAL ABUTMENT SYSTEM / DENTIN RESTORATION S | DZE | Substantially Equivalent | Dentin Implants Technologies , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Drill, Dental, Intraoral
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Bur, Dental
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
Updated July 5, 2012. 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.