Maverix Medical
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Risk Assessment

Developing molecular diagnostic tools that aim to triage lung cancer in patients to identify those in need of immediate care.

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Diagnosis

Endobronchial tissue-sampling instruments designed to help physicians obtain the tissue needed for an accurate diagnosis.

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Intervention

Minimally invasive devices for managing pleural effusions, restoring airway patency, and improving quality of life, along with an expanded suite of GI tools.

Explore the interventional portfolio
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Leadership

Maverix leadership combines decades of clinical, technical, and operating experience.

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Advisors

The Maverix Medical Advisory Board is comprised of leading pulmonary physicians.

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Most Recent Article
PR Newswire
August 20, 2026

Maverix Medical Announces FDA 510(k) Clearance for the Narwhal™ Cryo System

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PR Newswire
July 23, 2026
Maverix Names Carla Jung Chief Executive Officer to Lead Next Phase of Growth
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Regulatory Information

Maverix Medical devices are prescription-only and intended for use by trained physicians. Complete indications, contraindications, warnings, precautions, and directions for use are provided in each product’s Instructions for Use (IFU).

Electronic Instructions for Use (eIFU)

Instructions for Use are available electronically. Printed copies are available at no additional cost on request — contact Customer Care and we will send one within seven calendar days.

Access the eIFU library ↗

Requesting a Printed Copy

Email customercare@thoracent.com or call (888) 978-0232, Monday–Friday, 8:30–5:00 ET. Please include the product name, catalog number, and lot number shown on the device label.

Reporting an Adverse Event

To report a suspected adverse event or product complaint, contact customercare@thoracent.com. In the United States, adverse events may also be reported to the FDA through MedWatch.

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