Bioteque Corporation

Bioteque Corporation holds 3 FDA 510(k) medical device clearances, first cleared 2020, most recent 2025.

Top product codes for Bioteque Corporation

FGE — Gastroenterology, Urology3 devices

Recent clearances by Bioteque Corporation

K251019 — BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-GCode FGE·2025-12-22
K210419 — BIOTEQ Drainage Catheter BT-PDS-seriesCode FGE·2022-04-13
K200103 — BIOTEQ Drainage Catheter Set (One Step Type)Code FGE·2020-10-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.