27 results
·
34ms
·
Sources: EU EUDAMED, US FDA
MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00143531·
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001353·artVeneer life lower anteriors, UBXL, C2
NIH™
FDA UDI
MEDTRONIC, INC.·00613994964427·WVN CATH 001353 10PK 5440 6 80 NIH
NIH™
FDA UDI
MEDTRONIC, INC.·00763000199241·WVN CATH 001353 10PK 5440 6 80 NIH
OptiMesh Multiplanar Expandable Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7401001353·Short Foot Handbrace
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 17, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 6, 2025
SURGITRON IEC II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM
FDA 510(k)
FDA Class 2
·Neurology
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970607·
PHILIPS HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MKJ·May 19, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 17, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 6, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·January 16, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 9, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·October 20, 2025
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 8, 2021
2520274-2013-01407
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 13, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·February 25, 2011