510(k) Report

FDA applicant

Shenzhen Xiangtong Co., Ltd.

Shenzhen, CN3 decisions2023–20250 recalls

FDA records 3 decisions for Shenzhen Xiangtong Co., Ltd. (Shenzhen, CN) from 2023 to 2025: 3 510(k) clearances. All are in product code EIH (Powder, Porcelain). Since 2016 its 510(k)s took a median of 120 days from receipt to decision, against 114 for FDA’s reviews in the same codes and years. Its devices cite 3 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, dental panel, where it files most

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

FDA decisions per year

1in 2025

2023: 22025: 1
2023high 2 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Shenzhen Xiangtong Co., Ltd. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EIHPowder, Porcelain3decisions

How long do its 510(k) reviews take?

Since 2016, its 3 510(k)s took a median of 120 days from FDA’s receipt to its decision. For 510(k)s in the same product codes and years, FDA’s median was 114 days; 0 of its 3 were faster than that.

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K252789Glass CeramicShenzhen Xiangtong Co., Ltd. · 2025
  • K223192XT Stain/GlazeShenzhen Xiangtong Co., Ltd. · 2023
  • K223194Glass CeramicShenzhen Xiangtong Co., Ltd. · 2023

All 3 as Shenzhen Xiangtong Co., Ltd. →