12 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bengal Stackable Cage System
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517567932·CoRoent Ant TLIF PEEK, 9x10x28mm 4°
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017880·K-Wire, Double Ended, Trocar Point, Diameter Si...
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319721216·Buck Ear Curette 6-1/2" (16.3cm), size 3, blunt...
LIQUIBAND ULTIMA, LUT 003
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RES-Q INFANT WEDGE AND SLING
FDA 510(k)
FDA Class 1
·General Hospital
NOVOSTITCH CARTRIDGE 2-0
FDA Adverse Event
Injury
·CETERIX ORTHOPAEDICS, INC·Product code GAT·November 4, 2020
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020
MCLEAN-RING NASOJEJUNAL FEEDING TUBE SET
FDA Adverse Event
Injury
·COOK INC·Product code KNT·November 10, 2021
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·October 6, 2008
INRATIO2
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC·Product code GJS·July 19, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 26, 2013