Home › Device types › KOI
Stimulator, Nerve, Peripheral, Electric
FDA product code KOI · Class 2 · Anesthesiology
140
Registered devices
48
Adverse events
1
Recalls
29
510(k) clearances
Devices with this code
CARESCAPE B850 — GE Healthcare Finland OyTOF-CHAR_US — IDMEDTetraSens — Senzime AB (Publ.)NA — GE Healthcare Finland OyTetraGraph — Senzime AB (Publ.)NMT stimulate cable — Shenzhen Mindray Bio-Medical Electronics Co., Ltd.TwitchView2 Patient Cable 20' — BLINK DEVICE COMPANYHalyard — Avanos Medical, Inc.Hand adapter TOF3D — MIPM Mammendorfer Institut für Physik und Medizin GmbHWiTOF — IDMEDNMT sensor cable — Shenzhen Mindray Bio-Medical Electronics Co., Ltd.NA — GE Medical Systems Information Technologies, Inc.TwitchView2 Monitor — BLINK DEVICE COMPANYFisher & Paykel Healthcare — FISHER & PAYKEL HEALTHCARE LIMITEDFisher & Paykel Healthcare — FISHER & PAYKEL HEALTHCARE LIMITEDNA — GE Healthcare Finland OyFisher & Paykel Healthcare — FISHER & PAYKEL HEALTHCARE LIMITEDCARESCAPE B650 — GE Healthcare Finland OyiTOF — NERBIO PRIVATE LIMITEDNA — GE Healthcare Finland OyNMT cable — Shenzhen Mindray Bio-Medical Electronics Co., Ltd.TOF-MU — IDMEDCARESCAPE Software — GE Healthcare Finland OyTetraGraph Xcom — Senzime AB (Publ.)
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-04-09 | GE Healthcare, LLC | When the E-NMT-01 module is used in conjunction with the ElectroSensor, the Neuromuscular Transmission (NMT) values may indicate a deeper level of muscle relaxa |
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