9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
TRANSCUTANEOUS 800-OXYGEN MONITORS/801
FDA 510(k)
FDA Class 2
·Anesthesiology
IONOSTAR MOLAR
FDA 510(k)
FDA Class 2
·Dental
encevis (2.1)
FDA 510(k)
FDA Class 2
·Neurology
JGRKNT 1.0MM MINI 2-0 NDLS
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBI·May 30, 2014
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code OSI·November 20, 2012
PATIENT ROOM WALL SAVER RECL
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIV.·Product code FRK·September 10, 2010
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·February 26, 2012
PINNACLE MTL INS NEUT36IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·February 26, 2012
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·April 7, 2025