24 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Collaboration Live
FDA 510(k)
FDA Class 2
·Radiology
Broach
FDA UDI
Treace Medical Concepts, Inc.·00810111222679·Broach
NuVasive
FDA UDI
Nuvasive, Inc.·00887517949158·Universal Sizer, Angled - 8mm
Initia Total Hip System
FDA UDI
KYOCERA MEDICAL CORPORATION·04580810058485·"MXHO LINER 36-66/70
Size:36-66/68/70
Type:Elev...
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306823367·Marina Nasal Osteotome, 10mm, 18cm
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898307898·MXHO LINER 36-66/70
NUZONE NITRILE SURGICAL GLOVES POWDER FREE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SPAPLUS
FDA 510(k)
FDA Class 2
·Immunology
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 24, 2014
LASSO 2515 NAV VARIABLE CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·August 10, 2011
1.2X7MM BONE SCREWS,CROSS-PIN,SELF-T
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code HRS·July 1, 2013
TRILOGY 202
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·May 16, 2022
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·September 25, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·July 13, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·May 23, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 7, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·November 28, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·October 31, 2023
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·April 29, 2026
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·April 29, 2026