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Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Israel

FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Israel: 14 establishments

14 establishments in Israel are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Electrosurgical, Cutting & Coagulation & Accessories
Product code
GEI
Country
Israel

Makers of Electrosurgical, Cutting & Coagulation & Accessories in Israel

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Inmode Ltd.Yokneam Northern, IsraelManufacturer18January 15, 2026000api.fda.gov
Pollogen LtdTel Aviv, IsraelManufacturer6September 12, 2025000api.fda.gov
Alma Lasers Ltd.CAESAREA Northern, IsraelManufacturer3October 27, 2021000api.fda.gov
Endymed Medical LtdCaesarea Northern, IsraelManufacturer3June 10, 2025000api.fda.gov
ENTIRE MEDICAL LtdHERZLIYA Central, IsraelManufacturer2May 29, 2026000api.fda.gov
Novoxel Ltd.Netanya Tel Aviv, IsraelManufacturer2June 21, 2023000api.fda.gov
B.Y. Medimor LtdTiberias Northern, IsraelContract manufacturer0000api.fda.gov
El Global Trade Ltd.Netanya Central, IsraelManufacturer, Specification developer0000api.fda.gov
Humantouch Surgical Ltd.Netanya Central, IsraelComplaint file establishment, Manufacturer0000api.fda.gov
I. ShermanAcre Northern, IsraelContract manufacturer0000api.fda.gov
Resonetics, LLCOr Akiva Central, IsraelContract manufacturer0000api.fda.gov
Sharplight Technologies Ltd.RISHON LEZION Tel Aviv, IsraelManufacturer0000api.fda.gov
Usr Electronic Systems (1987) LtdKarmiel Northern, IsraelContract manufacturer0000api.fda.gov
Viora Ltd.Migdal HaEmek Northern, IsraelComplaint file establishment, Exporter to the US, Manufacturer0000api.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.