9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GERM TUBE SOLUTION
FDA 510(k)
FDA Class 1
·Microbiology
NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.
FDA 510(k)
FDA Class 2
·Physical Medicine
GGT PROCEDURE OR GAMMA GLUTAMYL TRANSFERASE PROCED
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SHILEY
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTO·September 1, 2010
FORTIFY DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 19, 2014
LCS FEM 65MM STD LT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code NJL·October 22, 2010
TWNFX TI 2.8 HS STR ANCHR 2 DRBRD NDL
FDA Adverse Event
Malfunction
·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code MBI·December 25, 2012
CPS SM SPDL WITH PINS 600LBF
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·February 26, 2021
CPS ANCHOR PLUG 14MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·February 26, 2021