FDA applicant
Zhengzhou PZ Laser Slim Technology Co., Ltd.
FDA records 10 decisions for Zhengzhou PZ Laser Slim Technology Co., Ltd. (Zhengzhou, CN) from 2018 to 2026: 10 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and NGX (Stimulator, Muscle, Powered, For Muscle…). Since 2016 its 510(k)s took a median of 90 days from receipt to decision, against 90 for FDA’s reviews in the same codes and years. Its devices cite 11 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
How often FDA has decided Zhengzhou PZ Laser Slim Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
5in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2018.
Planning a device like Zhengzhou PZ Laser Slim Technology…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Zhengzhou”
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