Eustachian tube balloon dilation device
FDA product code PNZ · Class 2 · 3 devices · 13 reports · 0 devices named in recalls
- ACCLARENT AERA EU061655Acclarent, Inc. · Eustachian tube balloon dilation device10 reports
- XprESS Ultra MSB&LLFStryker Corporation · Eustachian Tube Balloon Dilation Device2 reports
- Audion AET-100Stryker Corporation · Eustachian Tube Balloon Dilation Device1 report