Skip to the page

Data / Medical devices / Bur, Dental / Israel

FDA-registered makers of Bur, Dental in Israel: 9 establishments

9 establishments in Israel are registered with the FDA to make Bur, Dental (product code EJL). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Bur, Dental
Product code
EJL
Country
Israel

Makers of Bur, Dental in Israel

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abracadabra Implants Ltd.Or Yehuda Central, IsraelRepackager or relabeler, Specification developer0000api.fda.gov
Adin Dental Implant Systems Ltd.Afula Northern, IsraelManufacturer0000api.fda.gov
Bioline Dental Implant Systems LtdMigdal Tefen Northern, IsraelManufacturer0000api.fda.gov
Dentin Implants Technologies Ltd.Mizpe Aviv Northern, IsraelManufacturer, Specification developer0000api.fda.gov
Hi Tec Implants, Ltd.HERZLIA Tel Aviv, IsraelManufacturer0000api.fda.gov
MDT Micro Diamond Technologies LtdAFULA Northern, IsraelManufacturer0000api.fda.gov
Nova Implants LtdOr-Yehuda Tel Aviv, IsraelSpecification developer0000api.fda.gov
Paltop Advanced Dental Solutions LtdCaesarea Central, IsraelContract manufacturer0000api.fda.gov
Strauss & Co.Raanana Central, IsraelManufacturer0000api.fda.gov

Updated November 2, 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.