14 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ABSORBABLE SURGICAL GUT SUTURE*
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HANSATON stream remote 5.X
FDA UDI
Sonova AG·07613389610932·A mobile app for HANSATON hearing instruments
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011885018000·dentaform® Band, Tooth 36, Size 18
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011885018220·dentaform® Band, Tooth 36, Size 18/Roth 22
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011885018180·dentaform® Band, Tooth 36, Size 18/Roth 18
DAVOL ERCP CANNULA
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DURAHESIVE WAFER WITH FLANGE
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 11, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 11, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 11, 2024
MAGNUM TRISPIKE CUP 56ODX50ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 19, 2014
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·October 20, 2010
CHANNELSCOPE NEUROENDOSCOPE 30K
FDA Adverse Event
Injury
·MEDTRONIC NEUROSURGERY·Product code JXG·December 18, 2012
Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048 121711052 121712050 121712052 121712056 121722048 121722050 121722052 121722054 121722056 121722058 121722060 121722062 121731048 121731050 121731052 121731054 121731056 121731058 121731060 121731062 121732048 121732050 121732052 121732054 121732056 121732058 121732060 121732062 121732064 - Product Usage: The PINNACLE CUP devices are part of the Pinnacle Hip Solution for the anatomic reconstruction of the hip joint, which promotes prosthetic joint load and function.
FDA Enforcement
Class II
·Terminated·DePuy Orthopaedics, Inc.·January 13, 2021