Home › Device types › PNZ
Eustachian Tube Balloon Dilation Device
FDA product code PNZ · Class 2 · Ear, Nose, Throat
31
Registered devices
30
Adverse events
0
Recalls
9
510(k) clearances
Devices with this code
ACCLARENT PIVOT — ACCLARENT, INC.XprESS Ultra — STRYKER CORPORATIONACCLARENT AERA — ACCLARENT, INC.XprESS LoProfile — STRYKER CORPORATIONXprESS LoProfile — STRYKER CORPORATIONXprESS LoProfile — STRYKER CORPORATIONVenSure 4D Balloon Dilation System — Fiagon GmbHXprESS Pro — STRYKER CORPORATIONVenSure Light Balloon Dilation System — Fiagon GmbHACCLARENT PIVOT — ACCLARENT, INC.XprESS LoProfile — STRYKER CORPORATIONACCLARENT PIVOT — ACCLARENT, INC.XprESS Ultra — STRYKER CORPORATIONTubaVent® short — Spiggle & Theis Medizintechnik GmbHXprESS Ultra — STRYKER CORPORATIONAudion — STRYKER CORPORATIONACCLARENT PIVOT — ACCLARENT, INC.ACCLARENT PIVOT — ACCLARENT, INC.TubaInsert® - Type 45° — Spiggle & Theis Medizintechnik GmbHVenSure Nav Balloon Dilation System — Fiagon GmbHVenSure Balloon Dilation System — Fiagon GmbHACCLARENT PIVOT — ACCLARENT, INC.XprESS Ultra — STRYKER CORPORATIONXprESS Pro — STRYKER CORPORATION
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