Data / Medical devices / Israel / Adin Dental Implant Systems Ltd.
Adin Dental Implant Systems Ltd.: FDA-registered device maker in Afula Northern, Israel, 9 510(k) clearances
Adin Dental Implant Systems Ltd. is registered with the FDA (registration 3007518363) in Afula Northern, Israel. It lists 9 device types. The FDA files 9 510(k) clearances under its listings, the newest dated March 23, 2026. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3007518363
- Address
- Alon Tavor Industrial Zone POB 1128, Afula Northern, Israel, 1811101
- Owner or operator
- ADIN DENTAL IMPLANT SYSTEMS Ltd (10028570)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer
- First device listed
- February 12, 2009
- Registered through
- 2027
- Brand names listed
- ADIN UNIFIT DENTAL IMPLANT SYSTEM, Adin Dental Implants System, Adin Drill Stop Kits (Regular Long, Regular Short, Wide Long. Wide Short), Adin Short Implants, Adin Tri Step Drill Stop Kit, Anatomic Abutments, Angled Trans Mucosal Abutment Gauge, C-Type Ti Base and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Attachment, Precision, All | EGG | 1 | Manufacturer | accessdata.fda.gov |
| Bur, Dental | EJL | 1 | Manufacturer | accessdata.fda.gov |
| Controller, Foot, Handpiece And Cord | EBW | 1 | Exporter to the US | accessdata.fda.gov |
| Dental Abutment Design Software For Dental Laboratory | PNP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Dental Implant Surgical Tray | OFY | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Instruments, Dental Hand | DZN | 1 | 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 |
|---|---|---|---|---|---|---|
| March 23, 2026 | K252031 | Adin Long Dental Implant System | DZE | Substantially Equivalent | Adin Dental Implant Systems , Ltd. | accessdata.fda.gov |
| October 17, 2025 | K250178 | Adin Customized Abutments | NHA | Substantially Equivalent | Adin Dental Implant Systems , Ltd. | accessdata.fda.gov |
| December 29, 2023 | K223714 | UniFit Dental Implant System | DZE | Substantially Equivalent | Adin Dental Implant Systems , Ltd. | accessdata.fda.gov |
| July 8, 2022 | K212775 | Adin Short Implants | DZE | Substantially Equivalent | Adin Dental Implants Systems , Ltd. | accessdata.fda.gov |
| May 6, 2016 | K153111 | TOUAREG CloseFit UNP 2.75mmD | DZE | Substantially Equivalent | Adin Dental Implants Systems , Ltd. | accessdata.fda.gov |
| October 31, 2014 | K140293 | TOUAREG NP CLOSEFIT DENTAL IMPLANTS SYSTEM | DZE | Substantially Equivalent | Adin Dental Implants Systems , Ltd. | accessdata.fda.gov |
| May 24, 2012 | K112585 | TOUAREG CLOSEFIT DENTAL IMPANT SYSTEM | DZE | Substantially Equivalent | Adin Dental Implants System, Ltd. | accessdata.fda.gov |
| September 21, 2009 | K092758 | X-CUBE | EBW | Substantially Equivalent | Saeshin Precision Co., Ltd. | accessdata.fda.gov |
| December 19, 2008 | K081751 | ADIN DENTAL IMPLANTS SYSTEM | DZE | Substantially Equivalent | Adin Dental Implants System, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Instruments, Dental Hand
- All makers of Controller, Foot, Handpiece And Cord
- All makers of Dental Implant Surgical Tray
Updated March 23, 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.