ClearanceBrief
Company · US

Devoro Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2024. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QEWPeripheral Mechanical Thrombectomy With Aspiration5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 29, 2024K241207SmartClaw™ Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw™ Thrombectomy Catheter, 32 mm (FD0660-02)
Devoro Medical, Inc.
QEW
Nov 10, 2022K221391WOLF Thrombectomy™ SmartClaw Catheter
Devoro Medical, Inc.
QEW
Oct 19, 2021K210911WOLF Thrombectomy System, 14F
Devoro Medical, Inc.
QEW
Aug 27, 2021K210530WOLF Thrombectomy System, 6F
Devoro Medical, Inc.
QEW
Apr 27, 2020K200101WOLF Thrombectomy V System
Devoro Medical, Inc.
QEW

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes