Ventripoint Medical System Plus (VMS+)

Validation studies (1)

Reported performance (0 observations)

FDA source did not state a quantitative performance metric — non-reporting is itself the signal.

Each value carries its own analysis unit and task — never compare or pool across devices. Source: 510(k) summary PDF.

• re_clearance

  The FDA AI/ML device list shows a newer 510(k) K241222 (decision 2025-02-26) from Ventripoint Diagnostics Ltd. for a matching device line ("Ventripoint Medical System Plus (VMS+) 4.0") — a new clearance for the same line is a change event.

  first seen 2026-07-08 · k_number:K241222

• re_clearance

  The FDA AI/ML device list shows a newer 510(k) K191493 (decision 2019-10-16) from Ventripoint Diagnostics, Ltd. for a matching device line ("Ventripoint Medical System Plus (VMS+) 3.0") — a new clearance for the same line is a change event.

  first seen 2026-07-08 · k_number:K191493

• recall_reason_pattern

  Software/algorithm-related recall in product code IYN (Philips Ultrasound, LLC, initiated 2025-10-31): "Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining." Recalling firm is another firm in the same product code.

  first seen 2026-07-08 · recall res_event_number:97843

• recall_reason_pattern

  Software/algorithm-related recall in product code IYN (GE Medical Systems, LLC, initiated 2025-09-18): "The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica" Recalling firm is another firm in the same product code.

  first seen 2026-07-08 · recall res_event_number:97726

• recall_reason_pattern

  Software/algorithm-related recall in product code IYN (GE Medical Systems China Co., Ltd. Dev. Zone National Hi-Tech; No., initiated 2025-05-16): "GE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previou" Recalling firm is another firm in the same product code.

  first seen 2026-07-08 · recall res_event_number:96992

• recall_reason_pattern

  Software/algorithm-related recall in product code IYN (Siemens Medical Solutions USA, Inc., initiated 2024-08-15): "If ultrasound systems with software, are changed from factory default to : 1) Milliliters per second (ml/sec, mL/sec) or 2) Milliliters per minute (ml/min, mL/min); then systems wi" Recalling firm is another firm in the same product code.

  first seen 2026-07-08 · recall res_event_number:95254

Recall and MAUDE counts are product-code-level (reports aren't reliably attributable to one device). Signals are descriptive observables with sources — never a judgment that the device is unsafe or drifting. Snapshot 2026-07-08.