Data / Medical devices / Israel / Contipi Medical Ltd

Contipi Medical Ltd: FDA-registered device maker in Caesarea Haifa, Israel, 1 510(k) clearance

Contipi Medical Ltd is registered with the FDA (registration 3005674485) in Caesarea Haifa, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 8, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3005674485

Address

2 Alon Ha'Tavor St. Caesarea Industrial Park POB 3135, Caesarea Haifa, Israel, 3088900

Owner or operator

ConTIPI Medical Ltd (10089338)

Roles

Specification developer

First device listed

November 29, 2023

Registered through

2026

Brand names listed

ProVate

Devices it lists

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.

Compare with other makers

• All makers of Pessary, Vaginal

Updated July 8, 2019. 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.