353 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Vortex Surgical Inc
FDA UDI
Vortex Surgical, Inc.·00810123481392·25ga Kit (Forceps, Flat Lens, Retractable Edge ...
Vortex Surgical Inc
FDA UDI
Vortex Surgical, Inc.·00810123481385·23ga Kit (Forceps, Flat Lens, Retractable Edge ...
AELITE LS A2 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722A2F0·
AELITE LS A3 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722A3F0·
AELITE LS A1 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722A1F0·
AELITE LS A3.5 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722A35F0·
AELITE LS C2 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722C2F0·
AELITE LS B1 15tips/Fex Tube
FDA UDI
BISCO INC.·D757H722B1F0·
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·September 27, 2016
FEM-FELX, FEX-FLEX II FEMORAL ACCESS CANNULA WITH DURAFLO COATING
FDA 510(k)
FDA Class 2
·Cardiovascular
FIXODENT FEX
FDA Adverse Event
Other
·Product code KOL·May 20, 2009
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWY·July 17, 2014
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 17, 2014
RAYPEX 6
FDA Adverse Event
Malfunction
·VDW GMBH·Product code LQY·December 5, 2025
LIFEPAK(R) 15 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 2, 2024
POWERED ECHELON FEX 60
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GDW·May 15, 2012
NEXGEN LPS FEX ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·October 10, 2016
NEXGEN LPS-FEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER INC·Product code NJL·June 22, 2012
ALWAYS PURE COTTON WITH FEX FOAM
FDA Adverse Event
PROCTER & GAMBLE INC.·Product code HHD·October 22, 2021
UNKNOWN ZIMMER LPS-FEX FEMORAL TRIALS
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code LXH·April 2, 2008