13 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NuBODY Skin Toning Device
FDA 510(k)
FDA Class 2
·Neurology
VENFLON I 22GA 0.8 MM X 25MM
FDA Adverse Event
Malfunction
·Product code FOZ·August 4, 2021
VENFLON I 22GA 0.8 MM X 25MM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·December 31, 2019
ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL
FDA 510(k)
FDA Class 2
·Orthopedic
DISPENSER DP 20
FDA 510(k)
FDA Class 2
·General Hospital
PROG VALVE INLINE
FDA Adverse Event
Injury
·RAYNHAM·Product code JXG·June 3, 2019
CLICKX PEDICSCR Ø7 PREASSMBL L35 TAN GRE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code MNH·June 15, 2013
EASYTRAK 2
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code OJX·July 21, 2011
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·October 14, 2014
PERFORMER MULLINS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 20, 2023
PERFORMER MULLINS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 24, 2024
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·November 4, 2022
CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L e. 21-2120-0105-08L f. 21-2120-0105-12L g. 21-2120-0105-13L h. 21-2120-0105-14L i. 21-2120-0105-15L j. 21-2120-0105-17L k. 21-2120-0105-50L l. 21-2127-0105-02L m. 21-2127-0105-06L n. 21-2127-0105-50L
FDA Enforcement
Class I
·Terminated·Smiths Medical ASD Inc.·October 27, 2021