Bioteke Corporation (Wuxi) Co., Ltd. is one of 2152 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Bioteke Corporation (Wuxi) Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BioTeke® Multi-Drug Urine Test Cup, BioTeke Sterile Disposable Virus Sampling Kit
2
Total
2
Cleared
0
Denied
Bioteke Corporation (Wuxi) Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Wuxi City, CN.
Latest FDA clearance: Sep 2026. Active since 2022. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Bioteke Corporation (Wuxi) Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QSR Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Bioteke Corporation (Wuxi) Co., Ltd.
2 devices