43 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIGITAL FLAT PLANEL X-RAY DETECTOR / 1717SCC
FDA 510(k)
FDA Class 2
·Radiology
SPEACELABS MULTIGAS MODULE
FDA 510(k)
FDA Class 2
·Anesthesiology
MOLDEX-METRIC HEALTH CARE N95 PARTICULATE RESPIRATOR AND SURGICAL MASK, MODEL 1712
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 30, 2026
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code INB·October 31, 2011
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
POPULAR PLASTICS·Product code IKX·October 31, 2011
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code INB·November 18, 2011
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·June 8, 2012
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·July 5, 2012
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - AIBONITO·Product code FPA·May 21, 2013
FATHOM GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·June 13, 2011
LINOX SD 65/16
FDA Adverse Event
Malfunction
·BIOTRONIK, GMBH AND CO.·Product code LWS·August 15, 2008
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
POPULAR PLASTICS·Product code IKX·July 2, 2012
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·June 7, 2012
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·July 6, 2012
UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·October 23, 2017
UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 23, 2017
UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM
FDA Adverse Event
Death
·ZIMMER BIOMET, INC.·Product code JDI·October 23, 2017
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code INN·April 4, 2012