Reflow Medical, Inc.

2 product lines across 1 device categories: Microcatheters.

From reflowmedical.com, checked November 2026.

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

About Reflow Medical, Inc.

Reflow Medical, 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
coraFlex
Cora Flex Torqueable Microcatheter 14X135cm
Catheter Working Length: 135–150 cm; Guidewire Diameter: 0.01 in2Not stated
coraForce
Cora Force Torqueable Microcatheter 14x135cm
Catheter Working Length: 135–150 cm; Guidewire Diameter: 0.01 in2Not stated

Sales representatives

Reflow Medical, Inc. has not listed representatives here yet. Contact the company directly:

From reflowmedical.com, checked November 2026.

Outside their markets or no reply? Send us a request.

Work for Reflow Medical, Inc.? Add a rep and the areas they cover:

Frequently asked questions

What devices does Reflow Medical, Inc. make?

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

How do I contact a Reflow Medical, Inc. sales representative?

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

Does LA Vascular sell Reflow Medical, Inc. products?

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

Where do the Reflow Medical, 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