10 results
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17ms
·
Sources: EU EUDAMED, US FDA
SERUM IRON REAGENT SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CoRoent
FDA UDI
Nuvasive, Inc.·00887517368119·CoRoent® XL Ti, 12x18x40mm
LMDental
FDA UDI
LM-Dental·06438311220932·LM-SlimLift C4, Extraction
ERA® Implant Abutment Micro Ang. Base, 3mm Cuff (AP)
FDA UDI
STERNGOLD DENTAL LLC·00841549105104·Implant retained overdentures are an establishe...
EURO 45, ORDER-NO.: 2064
FDA 510(k)
FDA Class 2
·Dental
CAPNODURA COMBI & CAPNODURA PEDI CO2 DETECTOR
FDA 510(k)
FDA Class 2
·Anesthesiology
HEARTSTART XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·August 24, 2010
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 125 MM, Silicone, Sterile, Item 431190.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020