13 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PK Morcellator
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304500983·
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137510·Trial, 38 X 30, 17mm Height 16° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137527·Trial, 38 X 30, 19mm Height 16° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137534·Trial, 38 X 30, 21mm Height 16° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137497·Trial, 38 X 30, 13mm Height 16° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137503·Trial, 38 X 30, 15mm Height 16° Hyperlordotic
BARRIERPLUS PLATINUM POWDER-FREE SYNTHETIC POLYCHLOROPRENE SURGICAL GLOVES, MODELS 12544-125490
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER
FDA 510(k)
FDA Class 2
·Radiology
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 13, 2011
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
ORTHOPEDIC SALVAGE SYSTEM (OSS) IM STEM WITH SCREW POROUS PLASMA CEMENTED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·September 14, 2018