8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DORR HIP PROSTHESIS, ACETABULAR COMPON
FDA 510(k)
FDA Class 3
·Orthopedic
VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
FDA 510(k)
FDA Class 2
·Cardiovascular
UNDER BUTTOCKS DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 2, 2014
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·November 21, 2012
COULTER ® LH750
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code GKZ·September 23, 2010
TIBIAL INSERT FB SZ 2 RT 6MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code HSN·May 29, 2024
MENTOR TISSUE EXPANDER
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·February 4, 2019