510(k) Report

FDA applicant

Nanjing Jusha Display Technology Co., Ltd.

Nanjing, CN26 decisions2013–20230 recalls

FDA records 26 decisions for Nanjing Jusha Display Technology Co., Ltd. (Nanjing, CN) from 2013 to 2023: 26 510(k) clearances. Most are in product codes PGY (Display, Diagnostic Radiology) and LLZ (System, Image Processing, Radiological). Since 2016 its 510(k)s took a median of 63 days from receipt to decision, against 60 for FDA’s reviews in the same codes and years. Its devices cite 25 predicates, 12 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, radiology panel, where it files most

How often FDA has decided Nanjing Jusha Display Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

4in 2023

2013: 32014: 32015: 52019: 82020: 12022: 22023: 4
2013high 8 (2019) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Nanjing Jusha Display Technology Co., Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nanjing Jusha Display Technology Co.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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