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Cagent Vascular

Cagent Vascular wins FDA clearance for balloon catheter

April 27, 2020 By Sean Whooley

Cagent Vascular announced that it received FDA 510(k) clearance for its Serranator percutaneous transluminal angioplasty (PTA) serration balloon catheter. The FDA indication is for use of the Serranator for treating below-the-knee (BTK) lesions, making it the first and only angioplasty balloon with FDA clearance and CE Mark approval that embeds serration technology into a semi-compliant […]

Filed Under: 510(k), Catheters, Food & Drug Administration (FDA), Regulatory/Compliance, Vascular Tagged With: Cagent Vascular

Cagent Vascular closes $12m Series B

July 13, 2018 By Fink Densford

Cagent Vascular said today it closed a $11.9 million Series B round of financing to help support expand manufacturing and a limited launch of the company’s Serranator Alto angioplasty device. The round was led by two strategic investors and joined by Balestier Investments, Ben Franklin Technology Partners, Synergy Ventures and other private investors, the Wayne, Penn.-based […]

Filed Under: Business/Financial News, Vascular Tagged With: Cagent Vascular

7 medtech stories we missed this week: Dec. 8, 2017

December 8, 2017 By Danielle Kirsh

From Minimus Spine’s European distribution deal to Stimwave receiving FDA clearance, here are seven medtech stories we missed this week but thought were still worth mentioning. 1. Minimus Spine inks EU distribution deal Minimus Spine announced in a Dec. 4 press release that it has signed its first European distribution deal with Italian company Moss […]

Filed Under: 510(k), Cardiovascular, Diagnostics, Food & Drug Administration (FDA), Hospital Care, Pain Management, Regulatory/Compliance, Structural Heart Tagged With: Cagent Vascular, CSA Medical Inc., Dermacon, Elanix, Life Spine Inc., MedTech, Minimus Spine, Stimwave

FDA green-lights Cagent Vascular’s Serranator Alto PAD balloon catheter

February 27, 2017 By Brad Perriello

Cagent Vascular said today that it won 510(k) clearance from the FDA for its Serranator Alto balloon catheter, which is designed to treat peripheral artery disease. The Wayne, Pa.-based company bills its serration technology, created by co-founder and CMO Dr. Peter Schneider, as a way to improve arterial expansion during balloon angioplasty for PAD. The device’s […]

Filed Under: Food & Drug Administration (FDA), Regulatory/Compliance, Vascular Tagged With: Cagent Vascular, Peripheral

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July 1, 2022
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