510(k) Report

FDA applicant

Shenzhen Bestman Instrument Co., Ltd.

Shenzhen, CN2 decisions2010–20250 recalls

FDA records 2 decisions for Shenzhen Bestman Instrument Co., Ltd. (Shenzhen, CN) from 2010 to 2025: 2 510(k) clearances. All are in product code KNG (Monitor, Ultrasonic, Fetal). Its devices cite 2 predicates, 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Shenzhen Bestman Instrument Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2010: 12025: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Shenzhen Bestman Instrument Co., Ltd. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KNGMonitor, Ultrasonic, Fetal2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K090510Doppler Fetal Heartbeat Rate DetectorShenzhen Bestman Instrument Co., Ltd. · 20101cites it

What has FDA decided for it lately?

  • K242846Doppler FHR Detector (BF-500D+, BF-560)Shenzhen Bestman Instrument Co., Ltd. · 2025
  • K090510Doppler Fetal Heartbeat Rate DetectorShenzhen Bestman Instrument Co., Ltd. · 2010

All 2 as Shenzhen Bestman Instrument Co., Ltd. →