FDA applicant
Shenzhen Jamr Technology Co., Ltd.
FDA records 7 decisions for Shenzhen Jamr Technology Co., Ltd. (Shenzhen, CN) from 2020 to 2026: 7 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and KNG (Monitor, Ultrasonic, Fetal). Since 2016 its 510(k)s took a median of 177 days from receipt to decision, against 145 for FDA’s reviews in the same codes and years. Its devices cite 5 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 Shenzhen Jamr Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Shenzhen Jamr Technology Co., Ltd.’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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