FDA applicant
Chongqing Peninsula Medical Technology Co., Ltd.
FDA records 4 decisions for Chongqing Peninsula Medical Technology Co., Ltd. (Chongqing, CN) from 2018 to 2020: 4 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and OAP (Laser, Comb, Hair). Since 2016 its 510(k)s took a median of 228 days from receipt to decision, against 88 for FDA’s reviews in the same codes and years. Its devices cite 10 predicates, 2 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 Chongqing Peninsula Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2020
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2018.
Planning a device like Chongqing Peninsula Medical 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 “Chongqing”
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