The FDA has broadened the indications for MED-EL cochlear implants, allowing more adults with moderate-to-profound sensorineural hearing loss to qualify for the device.
The FDA has approved expanded indications for the MED-EL Cochlear Implant System, allowing more adults with bilateral moderate-to-profound sensorineural hearing loss to qualify.
MED-EL's cochlear implant system secures FDA approval for expanded use in adults with moderate-to-profound sensorineural hearing loss, setting a new industry standard.