News | Thrombectomy Devices | March 24, 2025

Imperative Care Expands Precision Thrombectomy Portfolio

Thrombectomy system is designed to efficiently maximize clot removal with a focus on minimizing blood loss. The 82 cm version of its Symphony 16F catheter receives FDA 510(k) clearance.

 Imperative Care catheter

March 24, 2025 — Imperative Care, Inc. recently announced U.S. Food and Drug Administration (FDA) 510(k) clearance of the 82 cm version of its Symphony 16F catheter. The catheter is designed to elevate care for patients with venous thrombosis, a serious condition caused by a blood clot forming in the veins of the legs or abdomen that can have a life-threatening impact if left untreated.

“Thrombectomy procedures have emerged as one of the most powerful treatments in medicine, restoring vital blood flow in minutes. Historically, peripheral vascular thrombectomy has lacked technologies that effectively address challenging clot and preserve vessel health for the patient,” said Doug Boyd, SVP and General Manager of Imperative Care’s Vascular business. “Imperative Care set out to transform vascular care through purpose-built precision thrombectomy technologies that combine large-bore power with a precisely controlled deep vacuum within the sterile field, along with a focus on minimizing blood loss. The Symphony Thrombectomy System has introduced precision thrombectomy to the market, and we are confident it will deliver faster, safer and more precise clot removal that will ultimately benefit patients impacted by devastating vascular diseases.”

Initial Cases 

The company also announced the successful completion of initial patient cases using the Symphony 16F 82cm catheter. Several of the initial cases were completed by Dr. Bennet George, Interventional Cardiologist at Vital Heart & Vein in Houston, Texas.

“In my early experience, I’ve been able to consistently achieve 97% clot removal in, on average, two passes, with minimal blood loss (<120ml) in less than ten minutes. With a large bore catheter and powerful deep vacuum, Symphony allows me to effectively treat highly challenging clot morphologies in minutes and in a blood-efficient way, ensuring the best possible outcomes for my patients,” said Dr. George. “The customized length of the 16F 82cm catheter gives me an additional capability to address both acute and organized clot in my venous procedures, and I look forward to its continued impact on the patients we treat.”

This latest innovation expands the Symphony Thrombectomy System offering to include 16F 82cm, 16F 117cm and 24F 85cm catheters.

Symphony has an integrated controller that delivers nearly three times the clot removal force compared to legacy aspiration systems1. Additionally, the system includes the ProHelix Mechanical Assist, a unique tool designed to facilitate clot ingestion, along with the Imperative Care Generator, the most powerful aspiration pump available on the market.

For more information on Imperative Care, please visit https://imperativecare.com.

 

[1] Data on file.


Related Content

News | FDA

July 28, 2026 — Implicity has been granted U.S. Food and Drug Administration (FDA) granted 510(k) clearance for its next ...

Home July 30, 2026
Home
News | FDA

July 24, 2026 — MannKind Corp. recently announced that the U.S. Food and Drug Administration (FDA) has approved Furoscix ...

Home July 28, 2026
Home
News | FDA

July 21, 2026 — ElectroWire Medical recently announced that the U.S. Food and Drug Administration (FDA) has granted 510 ...

Home July 23, 2026
Home
News | FDA

July 14, 2026 — Atrium Therapeutics, Inc. has announced that the U.S. Food and Drug Administration (FDA) has cleared its ...

Home July 14, 2026
Home
News | FDA

July 7, 2026 — W. L. Gore & Associates’ medical business recently announced that the U.S. Food and Drug Administration ...

Home July 13, 2026
Home
News | FDA

June 15, 2006 — Penumbra, Inc. has secured the CE Mark in Europe for Thunderbolt, further laying the groundwork for ...

Home June 15, 2026
Home
News | FDA

June 9, 2026.— Pentixapharm Holding AG has announced that the U.S. Food and Drug Administration (FDA) has cleared its ...

Home June 09, 2026
Home
News | FDA

April 16, 2026 — The U.S. Food and Drug Administration has granted 510(k) clearance to Royal Philips for its Philips ...

Home April 20, 2026
Home
News | FDA

April 7, 2026 —TRiCares SAS has received approval from the U.S. Food and Drug Administration (FDA) for an ...

Home April 09, 2026
Home
News | FDA

April 8, 2026 — Anumana, Inc. recently announced U.S. Food and Drug Administration (FDA) clearance of its ECG-AI ...

Home April 08, 2026
Home
Subscribe Now