Rapid Medical , Ltd. is one of 508 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Rapid Medical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Hyperdrive 35 Guidewire, Tigertriever 13 Ultra Revascularization Device, Drivewire 35 Guidewire
12
Total
10
Cleared
2
Denied
Rapid Medical , Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Yokneam, IL.
Latest FDA clearance: Sep 2026. Active since 2019.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP, Rapid Medical Ltd. and Rapid-Medical , Ltd.. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Rapid Medical , Ltd.
12 devices
Cleared
Sep 18, 2026
Hyperdrive 35 Guidewire
Cardiovascular
358d
Cleared
Aug 28, 2026
Tigertriever 13 Ultra Revascularization Device
Neurology
184d
Cleared
Jul 17, 2026
Drivewire 35 Guidewire
Neurology
214d
Cleared
Mar 12, 2026
Tigertriever 25 Revascularization Device
Neurology
171d
Cleared
Oct 06, 2025
Tigertriever 17 Ultra Revascularization Device
Neurology
132d
Cleared
Jul 11, 2024
Drivewire 24 Guidewire
Neurology
226d
Not Cleared
Feb 21, 2024
BraidE Embolization Assist Device
Cardiovascular
155d
Cleared
Apr 17, 2023
Tigertriever 21 Revascularization Device, Tigertriever 17 Revascularization...
Neurology
59d
Cleared
Jul 25, 2022
Tigertriever 13 Revascularization Device
Neurology
129d
Cleared
CT
Mar 23, 2021
Tigertriever and Tigertriever 17 Revascularization Devce
Neurology
105d
Cleared
Dec 14, 2020
Columbus Guidewire
Neurology
304d
Not Cleared
Apr 24, 2019
Comaneci, Comaneci Petit, Comaneci 17
Neurology
573d