FDA Device Intelligence
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Bronchoscope (Flexible Or Rigid)

FDA product code EOQ · Class 2 · Ear, Nose, Throat

1,186
Registered devices
31,113
Adverse events
160
Recalls
241
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-21Auris Health, IncDevice for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope lo
2025-12-04Intuitive Surgical, Inc.Due to probe bags that may have a compromised or incomplete sterile pouch seal.
2025-09-12Noah Medical CorporationDue to Users not having access to the Instructions for Use/User Manual due to it being password protected.
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.