25 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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AMERITEK BRACHYTHERAPY TEMPLATE
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040010983·Zirlux 16+ A3.5 100X25
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526189706·LEVAMED ACTIVE ANKLE SUP BLACK L I
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344361·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344354·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344316·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344347·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344323·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344378·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033344330·
SHARPS CONTAINER
FDA Adverse Event
Malfunction
·Product code MMK·January 13, 2026
ACUMATCH M-SERIES EXTRA-SMALL METAPHYSEAL SEGMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
LACTOSORB 5.0 MM WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
0009613348-2024-011581
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code DZE·September 2, 2024
0009613348-2024-011581
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code DZE·September 2, 2024
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 6, 2012
TI-DBLE LEAD CORT 5.0X50MM SCR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSB·July 9, 2021
TI-DBLE LEAD CORT 5.0X65MM SCR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSB·July 9, 2021
TI-DBLE LEAD CORT 5.0X80MM SCR IA5.0X80MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSB·July 9, 2021
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 19, 2013