57 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAS-One IR
FDA 510(k)
FDA Class 2
·Radiology
MULLINS-X PTV CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000
FDA 510(k)
FDA Class 1
·Radiology
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
CONSTALLATION VISION SYS
FDA Adverse Event
Malfunction
·ALCON -IRVINE TECH CTR·Product code HQC·October 6, 2014
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·April 2, 2021
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 9, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 30, 2018
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 11, 2024
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 30, 2018
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 20, 2020
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·November 12, 2020
SENRI
FDA Adverse Event
Injury
·KANEKA·Product code LIT·March 12, 2019
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 6, 2025
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 24, 2025
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020