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Bioteque Corporation

FDA Regulatory Profile

Bioteque Corporation appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 22, 2025.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251019BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-GDecember 22, 2025
K210419BIOTEQ Drainage Catheter BT-PDS-seriesApril 13, 2022
K200103BIOTEQ Drainage Catheter Set (One Step Type)October 9, 2020

FDA data resources