116 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GOBEN
FDA UDI
HUZHOU JUNDA INDUSTRY CO., LTD.·06979032640109·Elastic Bandages with Self Closure - 4 in x 5 y...
UNK LIQUID EMBOLIC
FDA Adverse Event
Death
·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021
UNK LIQUID EMBOLIC
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2021
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·September 8, 2017
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·November 29, 2022
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 22, 2013
UNK - RODS: VIPER
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·April 9, 2026
UNK - CONSTRUCTS: VIPER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·April 9, 2026
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·February 12, 2026
SUTURE, ABSORBABLE, SYNTHETIC
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·September 5, 2019
STERIS Kindest Kare Perineal Cleanser Incontinence System, packaged in 4-fl. oz. bottles (72 per case), Ready-To-Use, No-Rinse Solution, For Pediatric and Geriatric Use, For Hospital and Professional Use Only. The label shows the responsible firm to be STERIS Corporation, St. Louis, MO.
FDA Recall
Terminated
·Steris Corportion·Product code JD-01·April 28, 2004
Reedgyn disposable hysteroscope (Model RH-2S-01 and Model RH-2D-01)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BMT Medizintechnik GmbH
FDA UDI
BMT Medizintechnik GmbH·04251725202736·TWEEZERS COLLEGE, #17, 15 CM
MIS
FDA UDI
MIS Implants Technologies Ltd.·07290113990500·Conical Connection drill kit
TRANSONIC HEMODIALYSIS MONITOR, CARDIAC OUTPUT, MODEL HD01-CO
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FOTONA XD-2 DIODE LASER SYSTEM, MODEL MD01-2F
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HD01-SERIES TRANSONIC HEMODIALYSIS MONITOR (R%,QA,CO,QB,QB2)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Formthotics
FDA UDI
FOOT SCIENCE INTERNATIONAL LIMITED·09419430012452·3D Sample Pack Self Adhesive - M
HammerTech
FDA UDI
FUSION ORTHOPEDICS, LLC·00819034027170·HT PEEK Calibrated Drill Medium