10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
GRAM STAIN
FDA 510(k)
FDA Class 1
·Hematology
ReLine
FDA UDI
Nuvasive, Inc.·00195377021397·RELINE-C Ti Rod, 3.5x50mm Pre-Bent
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690121930·Femoral Posterior Augment Trial, Sz 3+, 5mm
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690121374·Femoral Augment Posterior, Size 3+, 5mm
VLP Mini-Mod Small Bone Plating System 1.5mm Plates and Screws
FDA 510(k)
FDA Class 2
·Orthopedic
HEMCON BANDAGE AND HEMCON BANDAGE OTC
FDA 510(k)
FDA Unclassified
·Unknown
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 2, 2014
JOSTENT GRAFTMASTER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MAF·November 21, 2012
REALIZE ADJ GASTRIC BAND STR
FDA Adverse Event
Malfunction
·OBTECH MEDICAL SARL_·Product code LTI·September 23, 2010
MENTOR SMOOTH ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·December 12, 2024