The Acclarent commitment

Acclarent is committed to offering training and support to help you successfully treat ETD.Treatment with the ACCLARENT AERA® device may allow more patients to regain normal ear function than with medical management alone.1

From individual support to practice management, our commitment includes:

  • Training the specialist on the system
  • Supporting the specialist in making this new procedure available
  • Providing the office staff with practice education on the procedure

Reimbursement information

Acclarent reimbursement hotline

Phone: 877-340-6466

Fax: 855-705-5092

Resources and support

For more information about ETD or ACCLARENT AERA®, click to view the following resources.

Why use ACCLARENT AERA®?

It was the first FDA-cleared balloon dilation intervention for ETD with a prospective, multicenter, randomized clinical trial.

Become
ACCLARENT AERA®
trained

Contact your local
representative or call
877-775-2789 if you are
a physician interested in
learning more about
ACCLARENT AERA® Eustachian
Tube Balloon Dilation System training.

Call
877-775-2789
to learn more
about training.

Reference

  1. ACCLARENT AERA® Eustachian Tube Balloon Dilation System Instruc­tions for Use. Irvine, CA: Acclarent, Inc.; 2018. IFU005146 Rev E.

Indications For Use

The ACCLARENT AERA® Eustachian Tube Balloon Dilation System is intended to dilate the Eustachian tube for treatment of persistent Eustachian tube dysfunction in adults ages 18 and older.

Important Safety Information

ACCLARENT AERA® is intended for use by physicians who are trained on Acclarent technology. Eustachian tube balloon dilation has
associated risks, including tissue and mucosal trauma, infection, or possible carotid artery injury. Prior to use, it is important to read
the Instructions for Use and to understand the contraindications, warnings, and precautions associated with these devices.

View ACCLARENT AERA® Instructions for Use