FDA Review Panel · EN

FDA 510(k) Ear, Nose & Throat Devices

About Ear, Nose, Throat Devices

FDA 510(k) ear, nose and throat (ENT) devices cover diagnostic and therapeutic equipment used in otolaryngology. The FDA review panel code is EN.

This category includes:

  • Hearing aids and amplifiers - air conduction, bone conduction and CROS systems
  • Cochlear implants - Class III devices (typically PMA, some 510k predicate paths)
  • ENT endoscopes - rigid and flexible nasopharyngoscopes, laryngoscopes
  • Surgical instruments - microdebriders, powered ENT systems
  • Audiometric systems - audiometers, tympanometers, OAE devices

59
Total
59
Cleared
145d
Avg days
2021
Since

FDA 510(k) Cleared Ear, Nose, Throat Devices

This page lists all 59 medical devices in the Ear, Nose, Throat specialty that have been submitted to the FDA through the 510(k) premarket notification process. Hearing aids, cochlear implants, ENT surgical instruments and endoscopes.

  • 59 devices cleared as substantially equivalent to a predicate device.
  • Average time to FDA decision: 145 days.
  • Records available from 2021 to the present.
  • Filter by product code using the sidebar to narrow results by device type.
59 Ear, Nose, Throat devices
1–12 of 59
Cleared Mar 20, 2026
Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D
K252050 · Olympus Medical Systems Corporation
EOB · Nasopharyngoscope (flexible Or Rigid) · 262d
Cleared Mar 16, 2026
Stealth AXiS™ ENT clinical application
K253395 · Medtronic Navigation, Inc.
PGW · Ear, Nose, And Throat Stereotaxic Instrument · 167d
Cleared Mar 02, 2026
KARL STORZ Mediastinoscopes and Instruments
K260003 · Karl Storz SE & CO. KG
EWY · Mediastinoscope, Surgical · 59d
Cleared Feb 19, 2026
Acclarent AERA Eustachian Tube Balloon Dilation System
K253612 · Acclarent, Inc.
PNZ · Eustachian Tube Balloon Dilation Device · 93d
Cleared Feb 10, 2026
NIM Essence™ EMG Endotracheal Tube (NIMEID060)
K251672 · Medtronic Xomed, Inc.
ETN · Stimulator, Nerve · 256d
Cleared Dec 12, 2025
FUJIFILM Ultrasonic Endoscope EB-710US
K250863 · Fujifilm Corporation
EOQ · Bronchoscope (flexible Or Rigid) · 266d
Cleared Dec 05, 2025
KARL STORZ Flexible Intubation Video Endoscope – Sterile (FIVE-S) (0916612)
K251731 · Karl Storz SE & CO. KG
EOQ · Bronchoscope (flexible Or Rigid) · 182d
Cleared Sep 23, 2025
Ion Endoluminal System (IF1000)
K252045 · Intuitive Surgical, Inc.
EOQ · Bronchoscope (flexible Or Rigid) · 85d
Cleared Sep 23, 2025
Bipolar applicator CelonProBreath (WB990310)
K252043 · Olympus Winter & Ibe GmbH
GEI · Electrosurgical, Cutting & Coagulation & Accessories · 85d
Cleared Sep 05, 2025
Ion Endoluminal System (IF1000)
K252528 · Intuitive Surgical, Inc.
EOQ · Bronchoscope (flexible Or Rigid) · 25d
Cleared Jun 23, 2025
EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-XP190)
K250862 · Olympus Medical Systems Corp.
EOQ · Bronchoscope (flexible Or Rigid) · 94d
Cleared Jun 13, 2025
FUJIFILM Endoscope Model EB-710P
K244017 · Fujifilm Corporation
EOQ · Bronchoscope (flexible Or Rigid) · 168d

How to use this database

This page lists 59 medical devices in the Ear, Nose, Throat specialty submitted to the FDA through the 510(k) premarket notification process. Of these, 59 were cleared as substantially equivalent to a predicate device. Average FDA review time: 145 days. Records from 2021 to the present.

You can use this list to:

  • Find predicate devices for a new 510(k) submission
  • Verify the clearance status of a specific device
  • Identify FDA product codes related to ear, nose, throat
  • Compare similar cleared devices within this category
  • Research manufacturers active in this specialty

Each entry includes: device name, 510(k) number, product code, manufacturer and FDA decision date. Click any device to view the full submission details.

This information is based on publicly available FDA data and is intended for informational purposes only. It may not reflect current market or regulatory status. Always verify critical information at accessdata.fda.gov.

Looking for a specific ear, nose, throat device? Search by device name, K-number or manufacturer.

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