Vantis Vascular, Inc.

2 product lines across 1 device categories: Microcatheters.

Is this your company? Claim this page to add product descriptions, indications, sizes and your sales reps by territory.

About Vantis Vascular, Inc.

Vantis Vascular, Inc. hasn't added a company description yet.

Microcatheters

Used in: Uterine Artery Embolization (UAE), Prostate Artery Embolization (PAE), Genicular Artery Embolization (GAE), Ovarian Vein Embolization, Varicocele Embolization, Transarterial Chemoembolization (TACE)

ProductSizes (FDA GUDID)ModelsMRI
CrossFAST(TM)
Integrated Microcatheter Guide Extension System, 5.5
—1Not stated
CrossFAST Integrated Microcatheter Advanced Delivery System
5.5, Catheter with Rapid Exchange Length
—1Not stated

Sales representatives

Vantis Vascular, Inc. has not listed representatives here yet. Send a request and we will route it to the right person for your country.

Work for Vantis Vascular, Inc.? Add a rep and the areas they cover:

FDA clearances and approvals

Frequently asked questions

What devices does Vantis Vascular, Inc. make?

Vantis Vascular, Inc. has 2 product lines in our library across 1 device category: Microcatheters.

Are Vantis Vascular, Inc. devices FDA cleared?

Our library lists FDA clearances and approvals for Vantis Vascular, Inc. products. The most recent is crossfast integrated microcatheter guide extension system cfm55 (510(k) K242276, 2024).

How do I contact a Vantis Vascular, Inc. sales representative?

Vantis Vascular, Inc. has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.

Does LA Vascular sell Vantis Vascular, Inc. products?

No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Vantis Vascular, Inc. or its representatives to buy.

Where do the Vantis Vascular, Inc. product sizes come from?

From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.

Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you