35 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Per-Q-Cath
FDA UDI
Bard Access Systems, Inc.·00801741127694·Catheter Placement Kit
CUSTOM PROCEDURE KIT
FDA UDI
MEDIVATORS INC.·40677964005723·The ENDO CARRY-ON Procedure Kit contains all of...
Lumalite
FDA UDI
PRYOR PRODUCTS·00761887002869·5-leg detach w support wheel
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 20, 2025
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 24, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 16, 2025
RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·August 15, 2024
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 20, 2025
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 16, 2025
TRUEBALANCE
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·August 13, 2014
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 18, 2025
Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·January 13, 2023
ZIMMER SKIN GRAFT MESHER
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·January 13, 2023
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
GOODBABY·Product code ITJ·March 12, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·February 2, 2011
GE OEC 9400
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 21, 2008
INSTINCT JAVA POLYAXIAL PEDICLE SCREW DG 40
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code NKB·July 12, 2016