16 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CATALOG NUMBER 111 (FACESHIELD)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Construction Irby Class B 21 - 36 Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588252902·Construction Irby Class B 21 - 36 Metal
KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL
FDA 510(k)
FDA Class 2
·Orthopedic
INMAN MEDICAL OIL EMULSION DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
NA
FDA UDI
STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT·Product code CBK·January 17, 2013
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NVZ·December 14, 2010
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·July 2, 2014
G7 OSSEOTI 3 HOLE SHELL 50MM D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·October 12, 2021
G7 DUAL MOBILITY LINER 40MM D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·October 12, 2021
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020