41 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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DEPUY RECLAIM REVISION HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SMARTSET
FDA UDI
DEPUY (IRELAND)·10603295168355·SmartSet ENDURANCE MV Medium Viscosity Bone Cem...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112656·BARRON CORNEAL PUNCH 8.5MM
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113904651·VICEROY Rod - 5.5 (D)5.5x(L)80mm
SEALED CALL CORD, 1/4" PLUG, 8FT, SF.
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828131384·SEALED CALL CORD, 1/4" PLUG, 8FT, SF.
TAMPAXTAMPONSPEARLFULLSIZESUPERUNSCNT18CT
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·October 15, 2025
SSD-5000 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BEHRING COAGULATION SYSTEM, MODEL BCS
FDA 510(k)
FDA Class 2
·Hematology
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
SIGMA PS CEM FEM SZ3 R
FDA Adverse Event
Injury
·Product code JWH·January 9, 2017
SMARTSET MV ENDURANCE 80G
FDA Adverse Event
Injury
·DEPUY CMW 9610921·Product code LOD·January 9, 2017
SIG MOD TIB TRAY CEM COCR 3
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code JWH·January 9, 2017
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·April 22, 2013
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·September 19, 2014
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·May 18, 2011
SMARTSET MV ENDURANCE 80G
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LOD·August 25, 2015
MAXIM PRIMARY TIBIAL BEARING 12MM X 63/67MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2023
SMARTSET MV ENDURANCE 80G
FDA Adverse Event
Injury
·DEPUY CMW 9610921·Product code LOD·December 3, 2015
SMARTSET MV ENDURANCE 80G
FDA Adverse Event
Injury
·DEPUY CMW - 9610921·Product code LOD·October 24, 2025
SIGMA PS CEM FEM SZ4 L
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code NJL·June 16, 2016