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PATIENT SPECIFIC TOTAL TALUS

FDA Adverse Event
Injury ·PARAGON 28, INC·Product code QNN·August 22, 2024

PATIENT SPECIFIC TALUS SPACER

FDA Adverse Event
Injury ·PARAGON 28, INC·Product code QNN·April 8, 2024

TOTAL TALUS

FDA Adverse Event
Injury ·RESTOR3D, INC.·Product code QNN·July 17, 2025

CUSTOM TATTR + STJ FUSION

FDA Adverse Event
Malfunction ·RESTOR3D, INC.·Product code QNN·August 21, 2025

TOTAL TALUS REPLACEMENT

FDA Adverse Event
Injury ·RESTOR3D, INC.·Product code QNN·September 3, 2025

PATIENT SPECIFIC TALUS SPACER

FDA Adverse Event
Injury ·PARAGON 28, INC·Product code QNN·May 10, 2024

PATIENT SPECIFIC TALUS SPACER

FDA Adverse Event
Injury ·PARAGON 28, INC·Product code QNN·May 8, 2024

PATIENT SPECIFIC TALUS SPACER

FDA Adverse Event
Injury ·PARAGON 28, INC·Product code QNN·April 8, 2024

RESTOR3D

FDA Adverse Event
Injury ·RESTOR3D·Product code QNN·October 6, 2023

RESTOR3D

FDA Adverse Event
Injury ·RESTOR3D·Product code QNN·October 6, 2023

RESTOR3D

FDA Adverse Event
Injury ·RESTOR3D·Product code QNN·October 6, 2023

PHYSICIAN DESIGNED CUSTOM ORTHOPEDIC IMPLANT

FDA Adverse Event
Injury ·4WEB, INC.·Product code QNN·March 2, 2026

PHYSICIAN DESIGNED CUSTOM ORTHOPEDIC IMPLANT

FDA Adverse Event
Injury ·4WEB, INC.·Product code QNN·February 28, 2025

PHYSICIAN DESIGNED CUSTOM ORTHOPEDIC IMPLANT

FDA Adverse Event
Injury ·4WEB, INC.·Product code QNN·February 3, 2025

TOTAL TALUS

FDA Adverse Event
Injury ·RESTOR3D, INC.·Product code QNN·January 31, 2025

Prosthesis, Total Talus Replacement, Metal

FDA classification
Prosthesis, Total Talus Replacement, Metal

Anne et Valentin

FDA registration
Anne et Valentin·2 products·🇫🇷 France

740 Series Multiparameter Monitor Software Version 3.0 Model Numbers: 740-1, 740M-1, 740-2T, 740M-2T, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS, 740-3NL, 740M-3NL, 740-3NN, and 740M-3NN CAS Medical Systems, Inc., Branford, Connecticut 06405 Indicated for use for non-invasive monitoring of blood pressure, oxygen saturation, pulse and temperature of adults, pediatric and neonatal patients, in the care of health professionals.

FDA Recall
Terminated ·CAS Medical Systems, Inc.·Product code MHX·June 24, 2008

DAYE (ANNE'S DAY LTD)

FDA registration
DAYE (ANNE'S DAY LTD)·3 products·🇬🇧 United Kingdom

ZHONGSHAN QUNN MEDICAL EQUIPMENT CO., LTD.

FDA registration
ZHONGSHAN QUNN MEDICAL EQUIPMENT CO., LTD.·3 products·🇨🇳 China