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Data / Medical devices / Ventilatory Effort Recorder / Israel

FDA-registered makers of Ventilatory Effort Recorder in Israel: 7 establishments

7 establishments in Israel are registered with the FDA to make Ventilatory Effort Recorder (product code MNR). 4 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
Ventilatory Effort Recorder
Product code
MNR
Country
Israel

Makers of Ventilatory Effort Recorder in Israel

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Itamar MedicalCAESAREA Haifa, IsraelManufacturer9September 5, 2025000api.fda.gov
Itamar Medical Ltd. (Alon)Caesarea Haifa, IsraelManufacturer9September 5, 2025000api.fda.gov
Dormotech Medical Ltd.Afula Northern, IsraelSpecification developer1January 8, 2025000api.fda.gov
S.L.P. Ltd.Tel-Aviv Tel Aviv, IsraelManufacturer1October 6, 2004000api.fda.gov
B.Y. Medimor LtdTiberias Northern, IsraelContract manufacturer0000api.fda.gov
Oridion Medical 1987 Ltd.Jerusalem, IsraelSpecification developer0000api.fda.gov
Sanmina- Sci Israel Medical Systems Ltd.Maalot-Tarshiha Northern, IsraelContract 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.