44 results
·
20ms
·
Sources: EU EUDAMED, US FDA
PM 2002 PROLINE/AEC
FDA 510(k)
FDA Class 2
·Dental
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964002197·Custom Procedure Kit
Intellijoint Surgical
FDA UDI
Provision·B504OM00001630·
intellijoint HIP®
FDA UDI
Intellijoint Surgical Inc·00628184001639·Screw, Pelvic, G2
SPECTRUM
FDA UDI
Ortho Arch Company Inc·D90980001631·SPECTRUM MINI LIGATURE CUTTER
GOLF BALL TITANIUM TYING FORCEP CVD 5MM
FDA UDI
DAUD JEE MFG. CO·G006DT5070001630·This instrument is used to grasp, retract, or s...
Preference 2
FDA UDI
SINTX Technologies, Inc.·M555244000163·Preference 2 Mini Set Screw Caddy Assembly
FlowLogic Agile
FDA UDI
SONENDO, INC.·00810209420024·FlowLogic Agile Shaping File 10/.04, 31mm
PROVEN KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AVL OPTI R ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ENDOCLAMP AORTIC CATHETER
FDA Adverse Event
Injury
·HEARTPORT INC.·Product code DWF·August 30, 2001
ENDOCLAMP AORTIC CATHETER
FDA Adverse Event
Injury
·HEARTPORT INC.·Product code DWF·August 30, 2001
ENDOCLAMP AORTIC CATHETER
FDA Adverse Event
Injury
·HEARTPORT INC.·Product code DWF·August 30, 2001
ENDOCLAMP AORTIC CATHETER
FDA Adverse Event
Injury
·HEARTPORT INC.·Product code DWF·August 30, 2001
IMPELLA 5.5
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code OZD·September 30, 2024
XMAX MOTOR
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code ERL·February 14, 2013
ZOOM CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·February 3, 2011
E SERIES DEFIBRILLATOR
FDA Adverse Event
Death
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 15, 2008
FEMUR SCREW STD 18MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022
UNKNOWN INTELLIJOINT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022