Neurent Medical , Ltd. - FDA 510(k) Cleared Devices

Neurent Medical, Ltd. is an innovative medical device company pioneering treatments for chronic inflammatory sino-nasal diseases. Based in Galway, Ireland, the company develops neuromodulation technologies that target hyperactive autonomic nerves to alleviate chronic rhinitis symptoms and improve patient quality of life.

Neurent Medical has received 1 FDA 510(k) clearance from 1 total submission. The company specializes exclusively in Ear, Nose, Throat devices, with its first and latest clearance both occurring in 2025. The company remains active, having achieved regulatory clearance within the past two years.

The company's flagship technology, NEUROMARK System, uses low-power radiofrequency energy to safely disrupt posterior nasal nerves. This minimally invasive approach targets the root cause of chronic rhinitis rather than managing symptoms alone. Clinical data demonstrates durable symptom relief with excellent patient tolerability and safety outcomes.

Explore Neurent Medical's cleared device names, product codes, and clearance dates in the FDA 510(k) database.