Home › Device types › MMX
Device, Percutaneous Retrieval
FDA product code MMX · Class 2 · Cardiovascular
143
Registered devices
404
Adverse events
1
Recalls
32
510(k) clearances
Devices with this code
SeQureTM Snare System — Lifetech Scientific (Shenzhen) Co., Ltd.Sympro Elite™ snare — Vascular Solutions, Inc.ONE Snare® — Merit Medical Systems, Inc.Atrieve™ Vascular Snare Kit — ARGON MEDICAL DEVICES, INC.Halo™ Single-Loop Microsnare Kit — ARGON MEDICAL DEVICES, INC.EN Snare® — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.Halo™ Single Loop Snare Kit — ARGON MEDICAL DEVICES, INC.EMPOWER™ — Merit Medical Systems, Inc.Quattro Elite™ snare — Vascular Solutions, Inc.ONE Snare® — Merit Medical Systems, Inc.Sympro Elite™ snare — Vascular Solutions, Inc.EXPRO ELITE — TELEFLEX INCORPORATEDSeQureTM Snare System — Lifetech Scientific (Shenzhen) Co., Ltd.Atrieve™ Vascular Snare Kit — ARGON MEDICAL DEVICES, INC.ONE Snare® — Merit Medical Systems, Inc.Atrieve™ Vascular Snare Kit — ARGON MEDICAL DEVICES, INC.Halo™ Single-Loop Microsnare Kit — ARGON MEDICAL DEVICES, INC.SYMPRO ELITE — TELEFLEX INCORPORATEDEXPRO ELITE — TELEFLEX INCORPORATEDMICRO ELITE — TELEFLEX INCORPORATEDONE Snare® — Merit Medical Systems, Inc.SeQureTM Snare System — Lifetech Scientific (Shenzhen) Co., Ltd.EN Snare® — Merit Medical Systems, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-07-17 | Cook Inc. | This remedial action is the result of six product complaints associated with separation of the snare from the distal tip of the wire. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.