15 results
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27ms
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Sources: EU EUDAMED, US FDA
INFUTEST 2000 INFUSION DEVICE ANALYZER
FDA 510(k)
FDA Class 2
·General Hospital
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980165·DeltaForm HD lower posteriors, M, BL1 -MADE IN ...
ZMR®
FDA UDI
Zimmer, Inc.·00889024364646·
ZMR®
FDA UDI
Zimmer, Inc.·00889024364653·
ZMR®
FDA UDI
Zimmer, Inc.·00889024364622·
ZMR®
FDA UDI
Zimmer, Inc.·00889024364639·
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025
SMART SAVERS POWDER FREE NITRILE EXAMINATION GLOVE (BLUE, WHITE, PINK AND GRAY)
FDA 510(k)
FDA Class 1
·General Hospital
Habib EndoHPB
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025
ASR ACETABULAR IMPLANT 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 27, 2013
MEDTRONIC
FDA Adverse Event
Injury
·MEDTRONIC·Product code NEK·February 2, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 2, 2014
Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025