510(k) Report

FDA applicant

Vingmed Sound, Inc.

Williamsburg, VA3 decisions1993–19970 recalls

FDA records 3 decisions for Vingmed Sound, Inc. (Williamsburg, VA) from 1993 to 1997: 3 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and ITX (Transducer, Ultrasonic, Diagnostic). 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, radiology panel, where it files most

How often FDA has decided Vingmed Sound, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vingmed Sound, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vingmed Sound, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Vingmed”

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