22 results · 24ms · Sources: EU EUDAMED, 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