8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MANAN GWI GUIDE WIRE INTRODUCER
FDA 510(k)
FDA Class 1
·Cardiovascular
BEMER Classic Set, BEMER Pro-Set
FDA 510(k)
FDA Class 2
·Physical Medicine
Persona Partial Knee
FDA 510(k)
FDA Class 2
·Orthopedic
MICRO INCISION VACUUM PHACO PACK
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·April 11, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·October 4, 2010
MINI TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·November 29, 2012
GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
FDA Enforcement
Class II
·Terminated·DePuy Orthopaedics, Inc.·January 19, 2022
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026