10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
TRYPTIC SOY AGAR (TSA) SLANT - PRODUCT #T8903 7ML
FDA 510(k)
FDA Class 1
·Microbiology
GC Initial™
FDA UDI
Gc America Inc.·J0228730571·GC Initial™ AL Dentin DB2, 20g
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Zimmer Knee Joint Replacement Prostheses MR Labeling
FDA 510(k)
FDA Class 2
·Orthopedic
STEM EXTENSION
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JWH·March 29, 2023
STEMMED NONAUGMENTABLE TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JWH·June 9, 2023
LCCK NEXGEN ARTICULAR SURFACE WITH LOCKING SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 9, 2022
PENUMBRA COIL 400
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·June 13, 2014
PUMP MMT-522LNAB PRDGM INS BL EN ML
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·October 15, 2010
COULTER® LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·December 13, 2012