11 results · 19ms · Sources: EU EUDAMED, US FDA

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TORQUE PLUS CATALOG 30120

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (BEARINGS / TRAYS)

FDA 510(k)
FDA Class 2 ·Orthopedic

MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANELS-AMOXICILLIN/CLAVULANATE POTASSIUM (AUGMENTIN)

FDA 510(k)
FDA Class 2 ·Microbiology

UNKNOWN PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 1, 2023

TOTAL ASR FEM IMP SIZE 51

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·May 27, 2014

PINN CAN BONE SCREW 6.5MMX40MM

FDA Adverse Event
Injury ·DEPUY WARSAW·Product code NDJ·November 15, 2012

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER CORP, MEDICAL DIV.·Product code FNL·September 9, 2010

NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·October 7, 2024

NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·October 7, 2024

REDUCED SIZE SCREW EXPANDABLE LEFT DISTAL FEMORAL 20CM REPLACEMENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 26, 2021

Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018