Imperative Care, Inc. is one of 16099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imperative Care, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Zoom 4S Catheter, Zoom System (Zoom 4S Catheter), Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System
18
Total
18
Cleared
0
Denied
Imperative Care, Inc. has 18 FDA 510(k) cleared neurology devices. Based in Sunnyvale, US.
Latest FDA clearance: Aug 2026. Active since 2018.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Imperative Care, Inc.
18 devices
Cleared
Aug 28, 2026
Zoom 4S Catheter
Neurology
140d
Cleared
Oct 30, 2025
Zoom System (Zoom 4S Catheter)
Neurology
122d
Cleared
CT
Aug 28, 2025
Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System
Cardiovascular
58d
Cleared
Aug 26, 2025
X-Wire Guidewire
Neurology
238d
Cleared
May 28, 2025
Zoom 7X Catheter
Neurology
243d
Cleared
May 14, 2025
Symphony™ Thrombectomy System
Cardiovascular
61d
Cleared
CT
Jan 14, 2025
Zoom System
Neurology
130d
Cleared
Jun 06, 2024
TracStar LDP Large Distal Platform
Neurology
59d
Cleared
Apr 02, 2024
Zoom 6F Insert Catheters
Cardiovascular
109d
Cleared
May 22, 2023
TracStar LDP Large Distal Platform
Neurology
27d
Cleared
May 17, 2022
Imperative Care Radial 088 Access System
Neurology
60d
Cleared
Sep 20, 2021
TracStar LDP Large Distal Platform
Neurology
66d