13 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Idys TLIF TiVac
FDA 510(k)
FDA Class 2
·Orthopedic
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970584·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970126·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970591·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172971116·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172971208·
NOTOUCH BREASTSCAN
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE
FDA 510(k)
FDA Class 1
·General Hospital
BLACKMAX-N-LP
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBB·October 17, 2014
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·June 21, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011
MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.
FDA Recall
Open, Classified
·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025
MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.
FDA Enforcement
Class I
·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025