65 results
·
66ms
·
Sources: EU EUDAMED, US FDA
INCORE Co., Ltd.
Manufacturer
🇰🇷 South Korea
INCORE CO., LTD.
FDA registration
INCORE CO., LTD.·8 products·🇰🇷 South Korea
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704711·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704896·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704872·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704841·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704858·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704889·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704865·
CORE-INJECTOR
FDA UDI
INCORE CO., LTD·08800035704728·
ARM & HAMMER SPINBRUSH SONIC BATTERY UNSPECIFIED
FDA Adverse Event
Malfunction
·CHURCH & DWIGHT CO., INC.·Product code JEQ·August 29, 2019
A&H SPINBRUSH TRULY RADIANT CLN + REFILLS CLUB PACK
FDA Adverse Event
Injury
·CHURCH & DWIGHT CO., INC.·Product code JEQ·January 20, 2021
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·September 3, 2025
UNKNOWN VICRYL RAPIDE SUTURE
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·March 20, 2023
Meridius Medical Europe Limited
Authorized representative
🇮🇪 Ireland·36 Manufacturers·720 Devices
Duk-In Cast
Device
EU MDR
·
Eu Md Class 1
·Duk-In Co., Ltd.·On the market
Duk-In Cast
Device
EU MDR
·
Eu Md Class 1
·Duk-In Co., Ltd.·On the market
Duk-In Cast
Device
EU MDR
·
Eu Md Class 1
·Duk-In Co., Ltd.·On the market
Duk-In Cast
Device
EU MDR
·
Eu Md Class 1
·Duk-In Co., Ltd.·On the market
Duk-In Cast
Device
EU MDR
·
Eu Md Class 1
·Duk-In Co., Ltd.·On the market