FDA applicant

Sony Corp. of America

North Attleboro, MA2 decisions1988–19890 recalls

FDA records 2 decisions for Sony Corp. of America (North Attleboro, MA) from 1988 to 1989: 2 510(k) clearances. Most are in product codes KQM (Camera, Surgical And Accessories) and FWB (Camera, Television, Surgical, Without Audio). 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, general and plastic surgery panel, where it files most

How often FDA has decided Sony Corp. of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sony Corp. of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sony Corp. of America by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Sony”

FDA records each applicant name separately; these may or may not be the same firm.

Sony Electronics, Inc. 8 Sony Medical Electronics Co. 8 Sony Medical Systems 6 Sony Corporation 1

Sony Corp. of America

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sony”