8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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G-Lok and G-Lok XL Extender
FDA 510(k)
FDA Class 2
·Orthopedic
PACK & PROPER PACK & PROPER, EAR-THERMOMETER PROBE CAP
FDA 510(k)
FDA Class 2
·General Hospital
ON CALL VIVID BLOOD GLUCOSE MONITORING SYSTEMS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PIP SZ. 10 PROXIMAL
FDA Adverse Event
Injury
·ASCENSION ORTHOPEDICS·Product code NEG·November 13, 2018
T7 DRIVER CANN AO
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code LXH·July 14, 2016
PEIVICOL ACELLULAR COLLAGEN MATRIX
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTL·March 13, 2013
PLUM A+ DRIVER EDITI
FDA Adverse Event
Malfunction
·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·September 26, 2014
X3 TRIATHLON CS INS SIZE1 9MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·June 21, 2011