38 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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2 PIECE MODULAR HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00131061·
Diamond D
FDA UDI
Keystone Industries·H66810131061·Denture Acrylic HC Dk Veined
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455791·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456002·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455821·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455814·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455807·
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918149035·Mayo Stand cover_29.5inx57in_140EA/CS
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455784·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033455838·
BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·May 25, 2022
STONELITH, MODEL V5
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EMIT II PLUS BENZODIAZEPINE ASSAY, MODEL 0SR9F229
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918183114·Mayo Stand Cover_29.5inx57in_Sterile_60ea/cs
LINER: MPACT FLAT PE HC LINER 36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·July 7, 2021
REVIVE SE 4.5MM OUS
FDA Adverse Event
Death
·MEDOS INTERNATIONAL SARL·Product code DXE·May 27, 2020
REVIVE SE 4.5MM OUS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code DXE·May 26, 2020
REVIVE SE 4.5MM OUS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code DXE·May 27, 2020
REVIVE SE 4.5MM OUS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code DXE·May 26, 2020