Bend IT Technologies, Ltd.

Bend IT Technologies, Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2019, most recent 2025.

Top product codes for Bend IT Technologies, Ltd.

Recent clearances by Bend IT Technologies, Ltd.

K252213 — Bendit17 MicrocatheterCode QJP·2025-12-03
K203842 — Bendit21 MicrocatheterCode QJP·2022-04-13
K200582 — Bendit2.7 Steerable MicrocatheterCode KRA·2020-06-25
K190126 — Bendit2.7 Steerable MicrocatheterCode DQO·2019-08-22

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