35 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRO-TOE HAMMERTOE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
K-WIRE
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·December 9, 2016
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981193751·Interbody, 11mm x 40mm x 14mm, 8 deg
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981201746·Interbody, 11mm x 40mm x 14mm, 8 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981208868·Trial, 11mm x 40mm x 14mm, 8 deg
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319720653·Rochester Pean Hemostatic Forceps 12" (30cm), c...
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925016927·MCGEE PISTON, S, 5.0MM LNG, 0.8MM DIAMETER
UniTip Catheter
FDA UDI
Unisensor AG·07640172971239·
RESOLUTION HEMOSTASIS CLIPPING DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SIMPLEXA INFLUENZA A H1N1 (2009) MODEL MOL2500
FDA 510(k)
FDA Class 2
·Microbiology
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7 HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·November 18, 2014
RADICAL-7
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·February 19, 2016
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Injury
·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Injury
·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014