35 results
·
36ms
·
Sources: EU EUDAMED, US FDA
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
FDA 510(k)
FDA Class 2
·Cardiovascular
SMITH & NEPHEW, INC. EXTERNAL FIXATION SYSTEM INSTRUMENTATION
FDA 510(k)
FDA Class 2
·Orthopedic
TRUSIGNAL SPO2 FINGERTIP SENSOR
FDA 510(k)
FDA Class 2
·Cardiovascular
G7 SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·March 28, 2013
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·April 24, 2026
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·February 27, 2013
MODULAR CUP SYSTEM, RIMCUP
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·January 21, 2026
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·March 1, 2013
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
THORACENTESIS TRAY WITH CATHETER
FDA Adverse Event
Malfunction
·CAREFUSION·Product code LRO·May 15, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 26, 2014
ACCUTNI AND ACCUTNI CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·May 20, 2011
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
G7 BONEMASTER LTD ACET SHL 58G
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019
G7 FINNED BM 3 HOLE SHELL 48C
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NDN·February 27, 2013