FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Acclarent AERA Eustachian Tube Balloon Dilation System

K Number: K253612 · Decision Feb 19, 2026
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
8
Applicant Total
45
Review Days
93

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Basic Information

Device Name
Acclarent AERA Eustachian Tube Balloon Dilation System
K Number
K253612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4180
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acclarent, Inc.
Date Received
November 18, 2025
Decision Date
February 19, 2026
Product Code
PNZ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PNZ Eustachian Tube Balloon Dilation Device

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PNZ), ordered by most recent decision date.

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Other Clearances by Acclarent, Inc.

K Number Device Name
K230742 ACCLARENT AERA Eustachian Tube Dilation System
K231862 TruDi® Navigation System V3 (FG-2000-00)
K221037 TruDi Shaver Blade
K201115 Next Generation Balloon Dilation System
K201174 TruDi Curette
K193453 TruDi Probe
K190525 RELIEVA ULTIRRA Sinus Balloon Catheter
K190532 TruDi NAV Wire
K183090 Relieva Tract Balloon Dilation System
K180948 TruDi NAV Suction Instruments
Search all 45 clearances from Acclarent, Inc. →