116 results · 35ms · Sources: EU EUDAMED, 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 SàRL CH·Product code NKB·April 9, 2026

UNK - CONSTRUCTS: VIPER

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL 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