8 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Ventana A Anterior Lumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System
FDA 510(k)
FDA Class 2
·Physical Medicine
PF4 ENHANCED SOLID PHASE ELISA
FDA 510(k)
FDA Class 2
·Hematology
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H)
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·May 13, 2024
BD PLASTIPAK¿ SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·July 29, 2021
VENTAK PRIZM HE VR
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 19, 2011
VITERION V100 BGM TELEHEALTH SYSTEM
FDA Adverse Event
Malfunction
·VITERION CORPORATION·Product code MWI·June 17, 2013