24 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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VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SYRINGE 0.5CCM 30GA 8MM BLS 100BX/500 AP
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·November 22, 2020
0.5 ML BD ULTRA-FINE II INSULIN SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·August 5, 2021
MODIFICATION TO XPS 3000 SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ALL-PRO 2010
FDA 510(k)
FDA Class 2
·Radiology
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118946·TLIF, 32mm X 10mm X 12mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118984·TLIF, 32mm X 10mm X 16mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118977·TLIF, 32mm X 10mm X 15mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118915·TLIF, 32mm X 10mm X 9mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118922·TLIF, 32mm X 10mm X 10mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118892·TLIF, 32mm X 10mm X 7mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118953·TLIF, 32mm X 10mm X 13mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118908·TLIF, 32mm X 10mm X 8mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118960·TLIF, 32mm X 10mm X 14mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118939·TLIF, 32mm X 10mm X 11mm, Convex 5°, PEEK
XPS® BUR GUARD - VISAO®
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ERL·April 22, 2016
XPS® BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 13, 2017
ACL ADVANCE
FDA Adverse Event
INSTRUMENTATION LABORATORY CO.·Product code JPA·July 13, 2005
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011