22 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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E-connect S Endo Motor with built-in Apex Locator
FDA 510(k)
FDA Class 1
·Dental
SHANCHUAN SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
SOF-TACT DIABETES MANAGEMENT SYSTEM; SOF-TACT GLUCOSE TEST STRIP; PRECISION CONTROL SOLUTIONS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ALPHA I INFLATABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·MENTOR UROLOGY, INC.·Product code FHW·May 30, 1997
ACUFEX TRAIL BLAZER (WITH NNULATED0 ( PROTOTYPE)
FDA Adverse Event
ACUFEX MICROSURGICAL, INC.·August 2, 1993
*
FDA Adverse Event
Injury
·DOW CORNING CORP.·Product code FTR·March 7, 1998
UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code JGS·August 5, 2011
ZIMMER REVERSE SHOULDER LINER
FDA Adverse Event
Injury
·ZIMMER INC·Product code KWT·June 26, 2013
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·October 27, 2014
ROTAWIRE AND WIRECLIP TORQUER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code MCX·June 18, 2019
ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code MCX·June 18, 2019
SMARTSET HV BONE CEMENT 40G
FDA Adverse Event
Injury
·DEPUY CMW - 9610921·Product code LOD·March 29, 2021
ZIMMER SKIN GRAFT MESHER
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL·Product code FZW·August 22, 2013
SMARTSET HV BONE CEMENT 40G
FDA Adverse Event
Injury
·DEPUY CMW - 9610921·Product code LOD·November 7, 2017
SMARTVIEW
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code LWP·January 11, 2019
DSX COLLIMATOR CART
FDA Adverse Event
Injury
·SOPHA MEDICAL·Product code HST·January 10, 1994
UNKNOWN SOLITAIRE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·January 31, 2023
PROMUS PREMIER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·October 7, 2019
PROMUS PREMIER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 30, 2019
PROMUS PREMIER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 30, 2019