15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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The ClearSight finger cuffs
FDA 510(k)
FDA Class 2
·Cardiovascular
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780372042·Integra® Jarit® Meyerding Finger Retractor, 7",...
CETRA
FDA UDI
Orthofix US LLC·18257200120345·1-LEVEL PLATE ASSEMBLY, 30MM
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101087·HELVESTON "BARBIE" RETRACTOR
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197187794·Caspar Distractor complete for vertical
cervic...
ATMOS S041 WOUND
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PATHFAST CTNI-II TEST, PATHFAST CTNI CALIBRATORS, PATHFAST SAMPLE DILUENT 2
FDA 510(k)
FDA Class 2
·Clinical Chemistry
AFFINITY DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 11, 2014
WALLGRAFT ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code JCT·August 4, 2011
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·June 11, 2013
AS VEGA PS FEMORAL COMP.CEMENTED F6N R
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·January 18, 2023
UNKNOWN
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 9, 2021
ZIMMON PANCREATIC STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 16, 2020
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·February 22, 2019
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.
FDA Enforcement
Class III
·Terminated·Invivo Corporation·October 28, 2020