Home › Device types › MFE
Agent, Injectable, Embolic
FDA product code MFE · Class 3 · Unknown
12
Registered devices
3,062
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Apollo Onyx — Micro Therapeutics, Inc.Onyx 18 — Micro Therapeutics, Inc.ONYX 18 — Micro Therapeutics, Inc.ApolloTM — Micro Therapeutics, Inc.ApolloTM — Micro Therapeutics, Inc.Apollo — Micro Therapeutics, Inc.Onyx 34 — Micro Therapeutics, Inc.OnyxTM Liquid Embolic System (LES) — Micro Therapeutics, Inc.Apollo — Micro Therapeutics, Inc.OnyxTM Liquid Embolic System (LES) — Micro Therapeutics, Inc.Apollo Onyx — Micro Therapeutics, Inc.ONYX 34 — Micro Therapeutics, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-01-11 | Micro Therapeutics, Inc. | European version of microcatheter were distributed within US which contain a different "Indications for Use". |
| 2024-01-11 | Micro Therapeutics, Inc. | European version of microcatheter were distributed within US which contain a different "Indications for Use". |
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