9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ANKLE FOOT ORTHOSIS
FDA 510(k)
FDA Class 1
·Physical Medicine
STRADIS
FDA UDI
STRADIS MEDICAL, LLC·M7526821639R11·CUSTOM SURGICAL KIT VEIN PACK
STRADIS
FDA UDI
STRADIS MEDICAL, LLC·M75268216391·CUSTOM SURGICAL KIT, PHLEBECTOMY PACK
ETHIX FEEDING TUBES POLYURETHANE/RADIOP.
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PERMITE DENTAL AMALGAM ALLOY
FDA 510(k)
FDA Class 2
·Dental
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·May 20, 2014
TAPERLOC POR FMRL 12.5X145
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·November 6, 2012
NOVAMAX LINK GLUCOSE MONITOR
FDA Adverse Event
Other
·NOVA BIOMEDICAL CORP·Product code NBW·August 26, 2010
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026