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Device, Nerve Conduction Velocity Measurement

FDA product code JXE · Class 2 · Neurology

205
Registered devices
93
Adverse events
1
Recalls
27
510(k) clearances

Devices with this code

Cascade — CADWELL INDUSTRIES, INC.ULTRA-DRIVE TOOL — Biomet Orthopedics, LLCCascade Elite — CADWELL INDUSTRIES, INC.Ultra-Drive® Tool — Biomet Orthopedics, LLCSierra Wave — CADWELL INDUSTRIES, INC.Ultra-Drive® Tool — Biomet Orthopedics, LLCULTRA-DRIVE TOOL — Biomet Orthopedics, LLCSierra Summit — CADWELL INDUSTRIES, INC.Cascade Pro — CADWELL INDUSTRIES, INC.ULTRA-DRIVE TOOL — Biomet Orthopedics, LLCCadwell Guardian — CADWELL INDUSTRIES, INC.IOMAX Extender Pod — CADWELL INDUSTRIES, INC.DPNCheck — IMPULSE MEDICAL TECHNOLOGIES, INC.ADVANCE — NeuroMetrix, Inc.ULTRA-DRIVE TOOL — Biomet Orthopedics, LLCSpinal Electrode Kit — Ad-Tech Medical Instrument CorporationDPNCheck, China — NeuroMetrix, Inc.ULTRA DRIVE III FOOTSWITCH — Biomet Orthopedics, LLCCascade — CADWELL INDUSTRIES, INC.Cadwell Guardian — CADWELL INDUSTRIES, INC.Disposable Goggle Foam — CADWELL INDUSTRIES, INC.DPNCheck — IMPULSE MEDICAL TECHNOLOGIES, INC.ULTRA-DRIVE TOOL — Biomet Orthopedics, LLCUltra-Drive® Tool — Biomet Orthopedics, LLC

Recent recalls

DateFirmReason
2012-04-18Biomet, Inc.Incorrect product picture label was on the product box.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.