417 results
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33ms
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Sources: EU EUDAMED, US FDA
TYRX ABSORBABLE ANTIBACTERIAL ENVELOPE
FDA Adverse Event
Injury
·TYRX, INC.·Product code FTL·August 8, 2019
TYRX ABSORBABLE ANTIBACTERIAL ENVELOPE
FDA Adverse Event
Injury
·TYRX, INC.·Product code FTL·October 3, 2019
TYRX ABSORBABLE ANTIBACTERIAL ENVELOPE
FDA Adverse Event
Injury
·TYRX, INC.·Product code FTL·October 2, 2019
TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Recall
Terminated
·TYRX Inc.·Product code FTL·June 29, 2016
TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Recall
Terminated
·TYRX Inc.·Product code FTL·June 29, 2016
TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Recall
Terminated
·TYRX Inc.·Product code FTL·June 29, 2016
TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Enforcement
Class II
·Terminated·TYRX Inc.·August 24, 2016
TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Enforcement
Class II
·Terminated·TYRX Inc.·August 24, 2016
TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
FDA Enforcement
Class II
·Terminated·TYRX Inc.·August 24, 2016
TYROS BIOPHARMA INC.
FDA registration
TYROS BIOPHARMA INC.·3 products·🇨🇦 Canada
Gynatrof(R)
FDA UDI
Tyros Biopharma Inc·00180266000058·Gynatrof is a personal lubricant, for vaginal a...
Gynatrof(R)
FDA UDI
Tyros Biopharma Inc·00180266000041·Gynatrof is a personal lubricant, for vaginal a...
AZURE XT DR MRI SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC SINGAPORE OPERATIONS·Product code NVZ·January 18, 2024
AIGIS
FDA Adverse Event
Injury
·TRYX, INC.·Product code FTL·October 6, 2017
Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws - 4.5, 5.5, 6.5, 7.5, 8.5, 9.5, 105 mm (all lengths); 2. Erisma-LP Screwdriver; 3. Erisma-LP T20 Wrench; 4. Erisma-LPT20 Snap Fit Tightening Wrench
FDA Recall
Terminated
·Clariance Inc·Product code NKB·July 1, 2019
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices
SUNGO Europe B.V.
Authorized representative
🇳🇱 Netherlands·1571 Manufacturers·20390 Devices