Bioteque Corporation is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Bioteque Corporation - FDA 510(k) Cleared Devices
Recent clearances: BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-G, BIOTEQ Drainage Catheter BT-PDS-series, BIOTEQ Drainage Catheter Set (One Step Type)
3
Total
3
Cleared
0
Denied
Bioteque Corporation has 3 FDA 510(k) cleared medical devices. Based in Taipei City, TW.
Latest FDA clearance: Dec 2025. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bioteque Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioteque Corporation
3 devices
Cleared
Dec 22, 2025
BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-G
Gastroenterology & Urology
264d
Cleared
Apr 13, 2022
BIOTEQ Drainage Catheter BT-PDS-series
Gastroenterology & Urology
426d
Cleared
Oct 09, 2020
BIOTEQ Drainage Catheter Set (One Step Type)
Gastroenterology & Urology
266d