# Devoro Medical, Inc.

- Location (FDA's records): Fremont, CA
- FDA decisions: 5 (2020–2024): 5 510(k) clearances
- Product codes: QEW (5)
- 510(k) review time since 2016: median 181 days, against 65 for FDA's reviews in the same codes and years (2 of 5 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 4 (4 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
- 880 Medical, LLC: 2 (https://510kreport.com/company/880-medical)

## Its most-cited devices
- K200101: WOLF Thrombectomy V System (2020), cited by 2
- K210911: WOLF Thrombectomy System, 14F (2021), cited by 1
- K221391: WOLF Thrombectomy™ SmartClaw Catheter (2022), cited by 1

## Recent decisions
- K241207: SmartClaw™ Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw™ Thrombectomy Catheter, 32 mm (FD0660-02) (May 29, 2024)
- K221391: WOLF Thrombectomy™ SmartClaw Catheter (Nov 10, 2022)
- K210911: WOLF Thrombectomy System, 14F (Oct 19, 2021)
- K210530: WOLF Thrombectomy System, 6F (Aug 27, 2021)
- K200101: WOLF Thrombectomy V System (Apr 27, 2020)

Source page: https://510kreport.com/company/devoro-medical