# Bend IT Technologies, Ltd.

- Location (FDA's records): Petach Tikva, IL
- FDA decisions: 4 (2019–2025): 4 510(k) clearances
- Product codes: QJP (2), DQO (1), KRA (1)
- 510(k) review time since 2016: median 174 days, against 115 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- MicroVention, Inc.: 1 (https://510kreport.com/company/microvention)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)

## Firms that cite its devices most
- Agile Devices, Inc.: 1 (https://510kreport.com/company/agile-devices)

## Its most-cited devices
- K203842: Bendit21 Microcatheter (2022), cited by 1
- K190126: Bendit2.7 Steerable Microcatheter (2019), cited by 1
- K200582: Bendit2.7 Steerable Microcatheter (2020), cited by 1

## Recent decisions
- K252213: Bendit17 Microcatheter (Dec 3, 2025)
- K203842: Bendit21 Microcatheter (Apr 13, 2022)
- K200582: Bendit2.7 Steerable Microcatheter (Jun 25, 2020)
- K190126: Bendit2.7 Steerable Microcatheter (Aug 22, 2019)

Source page: https://510kreport.com/company/bend-it-technologies