17 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZENITH, FEMORAL STEM ZENITH, DISTAL CENTRALIZER FOMORAL HEAD ACETABULAR INSERT
FDA 510(k)
FDA Class 2
·Orthopedic
LARGE CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010063915·6.5MM UNIVERSAL CANNULATED SCREW 80MM
SURGISTAR
FDA UDI
SURGISTAR, INC.·00878799006820·
DRIVESHAFT FOR SCREWDRIVER 90°
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·November 6, 2014
REHAB TNT, REHAB RAM, REHAB MAC, REHAB KIDSTER, BARIATRIC REHAB TNT AND REHAB RAM
FDA 510(k)
FDA Class 1
·Physical Medicine
ALBUMIN REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
GEAR COVER FOR SCREWDRIVER 90°
FDA Adverse Event
Malfunction
·SYNTHES OBERDORF·Product code DZI·November 6, 2014
SMR SHOULDER SYSTEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code PHX·May 18, 2026
OPTISENSE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014
12/14 ARTICUL 40MM M SPEC+15.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 21, 2013
MBT REVISION CEM TIB TRAY SZ 1
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code NJL·June 2, 2011
DRIVESHAFT FOR SCREWDRIVER 90°
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·November 6, 2014
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·August 18, 2014
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·July 11, 2014
SHAFT FOR 90° SCREWDRIVER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·June 20, 2019
UNKNOWN GAMMA3 LAG SCREW CASE 1
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code HWC·January 4, 2021
UNKNOWN GAMMA3 LAG SCREW CASE 2
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code HWC·January 4, 2021