27 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MB 103 MILLENNIUM BLADES
FDA 510(k)
FDA Class 1
·Ophthalmic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012529·Zirlux 16+ D3 95X22
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780811·LEVAMED ACTIVE ANKLE SUP SLVR R III
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0112330·Tap, 5.50mm, Fixed Sleeve
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077441·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077472·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077489·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077533·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077502·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077427·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077496·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077458·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077526·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077465·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077434·
AT WORK DRUG TEST, MODEL 9177T AWT
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PREFERENCE TREATMENT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 6, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 6, 2025
GMK REVISION TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 6, 2024