Home › Device types › OPR
Intrasaccular Flow Disruption Device
FDA product code OPR · Class 3 · Unknown
98
Registered devices
889
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
WEB Aneurysm Embolization System — Microvention, Inc.WEB — Microvention, Inc.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB — Microvention, Inc.WEB Aneurysm Embolization System — Microvention, Inc.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — Microvention, Inc.WEB — Microvention, Inc.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-09-21 | MICROVENTION INC. | Detachment controller, of an aneurysm embolization system, has an out of specification tunnel opening dimension, which may prevent the implant device pusher fro |
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