10 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798028·PEP REAGENT
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798042·Pep ReagentT
Stryker Facial iD Plating System
FDA 510(k)
FDA Class 2
·Dental
G2 EXPRESS FILTER SYSTEM - FEMORAL AND JUGULAR/SUBCLAVIAN DELIVERY KITS
FDA 510(k)
FDA Class 2
·Cardiovascular
LIGACLIP** ENDOSCOPIC CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 28, 2013
BASIC CONFIGURATION MODEL 6100 BASE
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIV·Product code FPO·January 13, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 5, 2014
Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick Electrosurgical/Bipolar Forceps/Reusable, Model #90-7004 (k) #K982705. The surgical device is package non-sterile into small plastic tubes. Olsen Medical Biopolar Reusable Bayonet Forceps and cords are intended for use in coagulating tissue during surgical procedures.
FDA Enforcement
Class II
·Terminated·PSC Industries Inc·July 18, 2012
Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick Electrosurgical/Bipolar Forceps/Reusable, Model #90-7004 (k) #K982705. The surgical device is package non-sterile into small plastic tubes. Olsen Medical Biopolar Reusable Bayonet Forceps and cords are intended for use in coagulating tissue during surgical procedures.
FDA Recall
Terminated
·PSC Industries Inc·Product code GEI·June 1, 2012