32 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Latex Powder Free Polymer Coated Examination Glove with Protein Labeling Claim of 50 Microgram or Less Per Gram of Glove
FDA 510(k)
FDA Class 1
·General Hospital
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304250710·
HAMILTON-T1
FDA UDI
Hamilton Medical AG·07630002801850·
OsteoMed
FDA UDI
OSTEOMED LLC·00842528123188·Logic Jr Distractor, 30mm Right
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311610060·
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000440·InSpan Slim, SP Plate, 12x39mm
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000433·InSpan Slim, SP Plate, 10x37mm
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000464·InSpan Slim, SP Plate, 16x43mm
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000419·InSpan Slim, SP Plate, 8x35mm
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000457·InSpan Slim, SP Plate, 14x41mm
InSpan®
FDA UDI
SPINEFRONTIER, INC.·00190361000426·InSpan Slim, SP Plate, 8x43mm
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321610060·
WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
IKOENGELO
FDA 510(k)
FDA Class 2
·Radiology
PRODIGY AUTOCODE
FDA Adverse Event
Malfunction
·OK BIOTECH CO., LTD.·Product code NBW·December 19, 2017
VEGA SPAN SPINOUS PROCESS PLATE SYSTEM
FDA Adverse Event
Injury
·SPINEFRONTIER INC.·Product code KWP·October 9, 2017
BELLAFILL DERMAL FILLER
FDA Adverse Event
Injury
·SUNEVA MEDICAL, INC.·Product code LMH·February 9, 2018
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013