Important Safety Information

The materials on this website are for your general educational information only. Information you read on this website cannot replace the relationship that you have with your healthcare professional. We do not practice medicine or provide medical services or advice as a part of this website. You should always talk to your healthcare professional for diagnosis and treatment.


NEUROMARK® device may be used in patients with recurring stuffy and/or runny nose. Your physician will need to determine if your condition is one that may benefit from NEUROMARK. Possible side effects include but are not limited to post-operative bleeding, pain or discomfort, allergic reaction to anesthesia or other medication administered during the procedure, and infection. Your condition may not respond to the treatment. To learn more about this procedure and potential risks, ask your physician.

INDICATIONS FOR USE: The NEUROMARK® System is indicated for use in otorhinolaryngology (ENT) surgery for creation of radiofrequency (RF) lesions to disrupt posterior nasal nerves in patients with chronic rhinitis.

Please see Instructions for Use (IFU) for a complete listing of warnings, precautions, and adverse events.


CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.