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Data / Medical devices / Medical Device Data System / Israel

FDA-registered makers of Medical Device Data System in Israel: 10 establishments

10 establishments in Israel are registered with the FDA to make Medical Device Data System (product code OUG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Medical Device Data System
Product code
OUG
Country
Israel

Makers of Medical Device Data System in Israel

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alma Lasers Ltd.CAESAREA Northern, IsraelManufacturer0000api.fda.gov
Alpha Omega Engineering Ltd.Nof HaGalil Northern, IsraelManufacturer0000api.fda.gov
Commwell Research And Development Ltdkfar saba Central, IsraelManufacturer0000api.fda.gov
Dreamed Diabetes LtdPetah Tikva Tel Aviv, IsraelManufacturer0000api.fda.gov
HealthwatchKfar Saba Central, IsraelManufacturer0000api.fda.gov
Itamar MedicalCAESAREA Haifa, IsraelManufacturer0000api.fda.gov
Mentaily Innovations LtdOr Yehuda Central, IsraelManufacturer0000api.fda.gov
Rocoto Ltd.Raanana Central, IsraelManufacturer0000api.fda.gov
SHL TeleMedicine InternationalTel-Aviv Tel Aviv, IsraelManufacturer0000api.fda.gov
TechsomedOr Yehuda Central, IsraelManufacturer0000api.fda.gov

Updated November 3, 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.