69 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Elevo® Kit Snoring Intervention Device
FDA 510(k)
FDA Class 2
·Dental
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776172848·SWISS CILIA FCPS -
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780361411·Integra® Miltex® Swiss Cilia and Suture Forceps...
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010235·
NA
FDA UDI
STRYKER CORPORATION·07613327056679·PEEK Multi-Function Handle
CASPIAN SPINAL SYSTEM, SCREWS, RODS, HOOKS, ROD CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE
FDA 510(k)
FDA Class 2
·Dental
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010280·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010273·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010266·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010259·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072010242·
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024
ARTIS Q ZEEGO
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026
ARTIS ZEEGO III (CHINA)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023
TOTAL ASR ACET IMP SIZE 46
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 20, 2013
UNKNOWN ZIMMER KNEE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 22, 2011