13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Ligence Heart
FDA 510(k)
FDA Class 2
·Radiology
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM
M/DN®
FDA UDI
Zimmer, Inc.·00889024041530·
ENDURANCE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295127963·ENDURANCE BROACH SIZE 5
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252105200·ceraMotion® Me Base Dentin Modifier lemon, 20 g...
Rocket IPC Insertion Set, Rocket IPC Mini Insertion Set
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
WATER FILLED TEETHER
FDA 510(k)
FDA Class 2
·Dental
LOQTEQ®
FDA UDI
aap Implantate AG·04042409363191·LOQTEQ® VA Volar Distal Radius Plate 2.5, broad...
DUROM ACETABULAR COMPONENT 54/48, CODE N
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·March 6, 2019
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC·Product code LYJ·December 4, 2008
COULTER® LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·September 16, 2011
GYNECARE MORCELLEX TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code HET·July 29, 2013
ECHELON ENDO LINEAR CUTTERS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 9, 2015