Data / Medical devices / Israel / Iq Implants Ltd
Iq Implants Ltd: FDA-registered device maker in Omer Southern, Israel, 1 510(k) clearance
Iq Implants Ltd is registered with the FDA (registration 3010610960) in Omer Southern, Israel. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 14, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010610960
- Address
- Taashur 9, Omer Southern, Israel, 84965
- Owner or operator
- IQ IMPLANTS LTD (10045610)
- Roles
- Manufacturer, Specification developer
- First device listed
- December 8, 2013
- Registered through
- 2026
- Brand names listed
- Aesthetic Abutments, Anatomic Angled Abutments 15 Degrees, Anatomic Angled Abutments 25 Degrees, Angled Abutments 15 Degrees, Angled Abutments 25 Degrees, Ball Abutments, Conical Drills with External Irrigation, Conical Drills with Internal Irrigation and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| November 14, 2013 | K130829 | IQ IMPLANTS; IQ IMPLANTS; IQ IMPLANTS ABUTMENTS | DZE | Substantially Equivalent | Iq Implants , 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 Drill, Dental, Intraoral
Updated November 14, 2013. 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.