FDA applicant

Jiangsu Trausim Medical Instrument

Changzhou City, Jaingsu Provicne, CN1 decision2014–20140 recalls

FDA records 1 decision for Jiangsu Trausim Medical Instrument (Changzhou City, Jaingsu Provicne, CN) in 2014: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Jiangsu Trausim Medical Instrument’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Jiangsu Trausim Medical Instrument by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Jiangsu Trausim Medical Instrument

Which product codes does it file in?

What has FDA decided for it lately?