46 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Focus DAILIES / Focus DAILIES Toric / Focus DAILIES Progressives, DAILIES AquaComfort Plus (DACP) / DACP FreshTech / DACP Toric / DACP Multifocal
FDA 510(k)
FDA Class 2
·Ophthalmic
SprintRay Standard Denture Teeth - B1
FDA UDI
Sprintray, Inc.·00850039704383·SprintRay Standard Denture Teeth is a light-cur...
E-A-RLINK™
FDA UDI
3M COMPANY·10080529191363·3M(TM) E-A-RLINK(TM) Foam plug-with-hole 1/2 in...
Conventional Lead Apron .5mm Xtra Large 25 X 40
FDA UDI
Flow X Ray Corporation·00843696123703·Conventional Lead Apron .5mm Xtra Large 25 X 40...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112618·BARRON CORNEAL PUNCH 7.5MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112496·BARRON VACUUM TREPHINE 7.5MM
OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER, MODEL 2100 AND DIGITAL DOLPHIN OPTICAL SENSOR, CLIP-ON FINGER PROBE, MOD
FDA 510(k)
FDA Class 2
·Cardiovascular
SIEMENS VIRTUAL SIMULATION (VSIM)
FDA 510(k)
FDA Class 2
·Radiology
HUMELOCK II
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·August 24, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·March 5, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·March 6, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·March 5, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·July 13, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·April 9, 2020
HUMELOCK REVERSED
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·March 2, 2020
SIZE 3 ACCOLADE II 127 DEG
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·November 3, 2020
OEM SS 20MM VENTED VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code LHI·December 14, 2020
OEM SS 20MM VENTED VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·March 4, 2021
HUMERIS
FDA Adverse Event
Injury
·FX SOLUTIONS·Product code PHX·March 6, 2020
OPTISENSE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014