9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
UniTip Catheter
FDA UDI
Unisensor AG·07640172973776·
SLICK SET
FDA 510(k)
FDA Class 2
·Anesthesiology
LED Light Therapy Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WECK AUTO ENDO5 APPLIER ML
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code FZP·October 5, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 30, 2014
TI MATRIX LOCKING CAP
FDA Adverse Event
Death
·SYNTHES BRANDYWINE·Product code NKB·December 20, 2012
DAVINCI SI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·December 29, 2022
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024