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Device, Percutaneous Retrieval
FDA product code MMX · Class 2 · Cardiovascular
143
Registered devices
398
Adverse events
1
Recalls
32
510(k) clearances
Devices with this code
EN Snare® — Merit Medical Systems, Inc.EXPRO ELITE — TELEFLEX INCORPORATEDEN Snare® — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.Halo™ Single Loop Snare Kit — ARGON MEDICAL DEVICES, INC.EN Snare® — Merit Medical Systems, Inc.EMPOWER™ — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.ONE Snare® — Merit Medical Systems, Inc.RECOVERY CONE® — Bard Peripheral Vascular, Inc.EN Snare® — Merit Medical Systems, Inc.EXPRO ELITE — TELEFLEX INCORPORATEDSeQureTM Snare System — Lifetech Scientific (Shenzhen) Co., Ltd.Atrieve™ Vascular Snare Kit — ARGON MEDICAL DEVICES, INC.Gunther Tulip — COOK INCORPORATEDMICRO ELITE — TELEFLEX INCORPORATEDSeQureTM Snare System — Lifetech Scientific (Shenzhen) Co., Ltd.ONE Snare® — Merit Medical Systems, Inc.Gunther Tulip — COOK INCORPORATEDSYMPRO ELITE — TELEFLEX INCORPORATEDQuattro Elite™ snare — Vascular Solutions, Inc.ONE 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. |
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