17 results
·
21ms
·
Sources: EU EUDAMED, US FDA
PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517564825·CoRoent Ant TLIF PEEK, 12x13x30mm 8°
ArgenPMMA 95x25-B3
FDA UDI
ARGEN CORPORATION, THE·D818123308·Crown And Bridge, Temporary, Resin
PG&E Class B 21 Trauma Burn BBP - OTS
FDA UDI
Certified Safety Manufacturing, Inc.·00766588233086·PG&E Class B 21 Trauma Burn BBP - OTS
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10887488278919·FORCEP
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981326142·Trial, 14x13mm, 10° Lordosis, 8mm Height, w/o D...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167310123308060·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167310123308120·
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·August 11, 2022
AIDA HD CONNECT WITH SMARTSCREEN / BLU-RAY DRIVE / SMARTSCREEN WITH BLU-RAY DRIVE
FDA 510(k)
FDA Class 2
·Radiology
LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 2, 2023
TI PANGEA(TM) LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·May 21, 2013
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
POWER PROCESSOR CENTRIFUGE
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JQC·September 28, 2006
AMISTEM H FEMORAL STEMS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 12, 2025
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
FDA Enforcement
Class I
·Ongoing·Covidien·November 8, 2023