Data / Medical devices / Israel / GP Implants Ltd
GP Implants Ltd: FDA-registered device maker in Netanya Central, Israel, 1 510(k) clearance
GP Implants Ltd is registered with the FDA (registration 3014270103) in Netanya Central, Israel. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 22, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014270103
- Address
- Beeri 12A St, Netanya Central, Israel, 4225910
- Owner or operator
- GP Implants Ltd (10056706)
- Roles
- Specification developer
- First device listed
- January 8, 2018
- Registered through
- 2026
- Brand names listed
- GP Implant System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | 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 |
|---|---|---|---|---|---|---|
| June 22, 2017 | K162299 | Spiral Shape Dental Implant System | DZE | Substantially Equivalent | Gp Implants | accessdata.fda.gov |
Compare with other makers
Updated June 22, 2017. 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.