510(k) Report

FDA applicant

Shanghai Samedical & Plastic Instruments Co., Ltd.

Shanghai, CN2 decisions2012–20250 recalls

FDA records 2 decisions for Shanghai Samedical & Plastic Instruments Co., Ltd. (Shanghai, CN) from 2012 to 2025: 2 510(k) clearances. Most are in product codes GXI (Probe, Radiofrequency Lesion) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). Its devices cite 2 predicates, 0 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, neurology panel, where it files most

How often FDA has decided Shanghai Samedical & Plastic Instruments Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2012: 12025: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Shanghai Samedical & Plastic Instruments Co., Ltd. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GXIProbe, Radiofrequency Lesion1decision
  • BSPNeedle, Conduction, Anesthetic (W/Wo Introducer)1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K241367RF CannulaShanghai Samedical & Plastic Instruments Co., Ltd. · 2025
  • K120475Anesthesia Conduction NeedlesShanghai Samedical & Plastic Instruments Co., Ltd. · 2012

All 2 as Shanghai Samedical & Plastic Instruments Co., Ltd. →