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Eustachian Tube Balloon Dilation Device
FDA product code PNZ · Class 2 · Ear, Nose, Throat
31
Registered devices
31
Adverse events
0
Recalls
9
510(k) clearances
Devices with this code
ACCLARENT PIVOT — ACCLARENT, INC.ACCLARENT PIVOT — ACCLARENT, INC.XprESS Pro — STRYKER CORPORATIONACCLARENT AERA — ACCLARENT, INC.VenSure Balloon Dilation System — Fiagon GmbHXprESS Pro — STRYKER CORPORATIONACCLARENT AERA — ACCLARENT, INC.XprESS LoProfile — STRYKER CORPORATIONVenSure Light Balloon Dilation System — Fiagon GmbHXprESS Ultra — STRYKER CORPORATIONACCLARENT PIVOT — ACCLARENT, INC.TubaInsert® - Type 45° — Spiggle & Theis Medizintechnik GmbHXprESS Ultra — STRYKER CORPORATIONACCLARENT PIVOT — ACCLARENT, INC.XprESS LoProfile — STRYKER CORPORATIONXprESS LoProfile — STRYKER CORPORATIONNuVent — MEDTRONIC XOMED, INC.TubaVent® balloon dilatation system — Spiggle & Theis Medizintechnik GmbHAudion — STRYKER CORPORATIONTubaVent® short wide — Spiggle & Theis Medizintechnik GmbHXprESS LoProfile — STRYKER CORPORATIONXprESS Pro — STRYKER CORPORATIONXprESS Ultra — STRYKER CORPORATIONXprESS Ultra — STRYKER CORPORATION
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