Hangzhou Ruidi Biotechnology , Ltd. is one of 1971 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Hangzhou Ruidi Biotechnology , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Steep Pulse Ablation Instrument (including Disposable Sterile Steep Pulse Probe) (SPA-C02)
1
Total
1
Cleared
0
Denied
Hangzhou Ruidi Biotechnology , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Hangzhou, CN.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hangzhou Ruidi Biotechnology , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beijing Tigermed-Jyton Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Hangzhou Ruidi Biotechnology , Ltd.
1 devices