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FDA product code GXR · Class 2 · Neurology

1,378
Registered devices
210
Adverse events
1
Recalls
29
510(k) clearances

Devices with this code

MatrixNEURO — Synthes GmbHTHINFLAP — BIOMET MICROFIXATION, INCTHINFLAP SYSTEM 5/PK — BIOMET MICROFIXATION, INCLeforte Neuro System Bone Plate — Jeil Medical CorporationNA — MEDTRONIC, INC.1.5MM SYSTEM — BIOMET MICROFIXATION, INC1.5MM SYSTEM — BIOMET MICROFIXATION, INCRAAS Cranial Plating System — ALLIANCE PARTNERS LLC2.0MM SYSTEM — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INC"2.0MM" SYSTEM — BIOMET MICROFIXATION, INC1.5MM SYSTEM — BIOMET MICROFIXATION, INC1.5MM SYSTEM — BIOMET MICROFIXATION, INC1.5MM SYSTEM — BIOMET MICROFIXATION, INC"2.0MM" SYSTEM PLATE — BIOMET MICROFIXATION, INC"2.0MM" SYSTEM — BIOMET MICROFIXATION, INCLeforte Neuro System Bone Plate — Jeil Medical CorporationRAAS Cranial Plating System — ALLIANCE PARTNERS LLCMatrixNEURO — Synthes GmbHNA — Synthes GmbHCMF SYSTEM — BIOMET MICROFIXATION, INCNeuroPro® Low Profile — Kinamed, Inc.MatrixNEURO — Synthes GmbHDELTA — Stryker Leibinger GmbH & Co. KG

Recent recalls

DateFirmReason
2021-06-02Medtronic NeuromodulationExcess nylon flash on the clip.

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