115 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL M4735A
FDA 510(k)
FDA Class 3
·Cardiovascular
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00171251·
ShaRing + Litening Rods (3) for Aribex Nomad
FDA UDI
CLIKTECH LLC·00856200001725·ShaRing + Litening Rods (3) for Aribex Nomad
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756556378·Pediatric Anesthesia Circuit
BETA-TITANIUM
FDA UDI
Gc Orthodontics America Inc.·D78873K30017251·BETA-TITAN KEYHOLE 17X25 30MM
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194464840·VERTEGLIDE 4.5 ROD COCR, 500MM, 60MM FUSION, OF...
Sonova Brand
FDA UDI
Sonova AG·07613389477047·myPhonak Junior app
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194478564·VERTEGLIDE 4.5 ROD COCR, 500MM, 90MM FUSION, OF...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194478595·VERTEGLIDE 5.5 ROD COCR, 500MM, 150MM FUSION, O...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194464918·VERTEGLIDE 5.5 ROD COCR, 500MM, 120MM FUSION, O...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194478588·VERTEGLIDE 5.5 ROD COCR, 500MM, 90MM FUSION, OF...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194464888·VERTEGLIDE 5.5 ROD COCR, 500MM, 60MM FUSION, OF...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194464871·VERTEGLIDE 4.5 ROD COCR, 500MM, 120MM FUSION, O...
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194478571·VERTEGLIDE 4.5 ROD COCR, 500MM, 150MM FUSION, O...
LIFECARD CF COMPACT RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
HWA (AND) SILKTEX POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
MaxTorque™
FDA UDI
TORNIER, INC.·00846832054213·
MINIMED QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·October 4, 2024
SIGMA HP FEM NOTCH IMPACTOR
FDA Adverse Event
Malfunction
·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code LXH·January 30, 2014
EZ-IO POWER DRIVER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code FMI·December 14, 2020