510(k) Report

FDA applicant

Bose Corporation

Framingham, MA2 decisions2018–20210 recalls

FDA records 2 decisions for Bose Corporation (Framingham, MA) from 2018 to 2021: 1 510(k) clearance and 1 De Novo grant. All are in product code QDD (Self-Fitting Air-Conduction Hearing Aid…). Its devices cite 1 predicate, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Bose Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2018: 12021: 1
2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Bose Corporation by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • QDDSelf-Fitting Air-Conduction Hearing Aid, Prescription2decisions

Who builds on its devices?

Later devices cite its devices 11 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K211008Bose SoundControl Hearing AidsBose Corporation · 20216cite it
  • DEN180026Bose Hearing AidBose Corporation · 20185cite it

What has FDA decided for it lately?

  • K211008Bose SoundControl Hearing AidsBose Corporation · 2021
  • DEN180026Bose Hearing AidBose Corporation · 2018

All 2 as Bose Corporation →