13 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DIGITAL ELECTROCARDIOGRAPHS
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814749·GENUMEDI EXTRA WIDE SAND SIZE VI
CASCADIA™ Interbody System
FDA UDI
VB Spine LLC·10888857554702·Trial Size 16x20x11 mm, Convex
COHESION BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
CANON FULL AUTO TONOMETER TX-F
FDA 510(k)
FDA Class 2
·Ophthalmic
HAHN TAPERED 7.0 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 11, 2023
HAHN TAPERED IMPLANT Ø7.0 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·September 23, 2025
HAHN TAPERED IMPLANT Ø7.0 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 19, 2024
AMISTEM H CEMENTLESS STEM #4 LAT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code MEH·February 9, 2015
ZERO TIP?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code FFL·May 22, 2013
ENTRUST VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·June 14, 2011
T4/WD08/HD/ADULT/28/BH16/AT903/U2222C/COM/U550 9153639974
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·October 2, 2015
AMISTEM H, HA COATED STEM SIZE 4 LAT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 19, 2016