9 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA
FDA 510(k)
FDA Class 2
·Orthopedic
VICRYL* POLYGLACTIN 730 ABSORBABLE STAPLES/STAPLER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CUI DORSAL COLUMELLA PROSTHESIS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SM HYBRID GLENOID BASE 4MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·August 19, 2022
N/A
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NIK·February 15, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 29, 2014
UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER INC.·Product code DHA·January 19, 2011
VERSA-DIAL 46X21X50 HUM HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·April 6, 2022
INTERCHANGEABLE HUMERAL ASSEMBLY FOR CEMENTED USE ONLY SMALL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·August 23, 2022