2,884 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POLARIS URETERAL STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·July 21, 2020
LUMENIS SLIMLINE 200 D/F/L
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·October 19, 2023
OCCLUDER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EYB·January 20, 2022
SHOCKPULSE-SE LITHOTRIPSY SYSTEM (REUSAB
FDA Adverse Event
Malfunction
·GYRUS ACMI INC·Product code FEO·November 4, 2020
SOF-FLEX MULTI-LENGTH URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·June 16, 2023
SENSOR
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code EZB·September 30, 2019
Voriconazole Test System
FDA classification
FDA Class 2
·Voriconazole Test System
PUL Technologies LLC.
FDA registration
PUL Technologies LLC.·2 products·🇺🇸 United States
PUR BIOLOGICS, LLC
FDA registration
PUR BIOLOGICS, LLC·1 product·🇺🇸 United States
MOTO PFJ System
FDA 510(k)
FDA Class 2
·Orthopedic
PK J-HOOK
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Covidien Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens
FDA Enforcement
Class II
·Terminated·Medtronic·December 28, 2016
D-PUB Electronic & Technology Co. Ltd
FDA registration
D-PUB Electronic & Technology Co. Ltd·3 products·🇨🇳 China
KneeTec PFJ
FDA UDI
CORIN LTD·05056139210242·KneeTec PFJ Femoral implant Left Size 1
KneeTec PFJ
FDA UDI
CORIN LTD·05056139221262·Reamer Dia. 9mm
KneeTec PFJ
FDA UDI
CORIN LTD·05056139221545·Femoral Drill Guide S4 Left
KNEETEC PFJ
FDA UDI
TORNIER·03700386937798·
KneeTec PFJ
FDA UDI
CORIN LTD·05056139221491·Femoral Drill Guide S3 Right
KneeTec PFJ
FDA UDI
CORIN LTD·05056139221088·Positioning Frame Right
KneeTec PFJ
FDA UDI
CORIN LTD·05056139221071·EM Alignment Guide