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Data / Medical devices / Israel / Virility Medical Ltd.

Virility Medical Ltd.: FDA-registered device maker in Hod Hasharon Central, Israel, 2 510(k) clearances

Virility Medical Ltd. is registered with the FDA (registration 3017709633) in Hod Hasharon Central, Israel. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 6, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3017709633
Address
24 Hanagar St., Hod Hasharon Central, Israel, 4527713
Owner or operator
Virility Medical Ltd. (10090420)
Roles
Complaint file establishment, Manufacturer
First device listed
March 26, 2024
Registered through
2026
Brand names listed
in2, in2 Smart

Devices it lists

DeviceProduct codeClassRoleSource
Non-Implanted Electrical Stimulation Device For Management Of Premature EjaculationQRC2Complaint file establishment, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 6, 2026K252809in2 Smart (in2S)QRCSubstantially EquivalentVirility Medical , Ltd.accessdata.fda.gov
May 1, 2023K223595vPATCHQRCSubstantially EquivalentVirility Medical , Ltd.accessdata.fda.gov

Updated April 6, 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.