23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Sunkingdom Applanation Tonometer SK-R, SK-T, SK-Q
FDA 510(k)
FDA Class 2
·Ophthalmic
Bernafon
FDA UDI
Bernafon AG·05711584086018·ZR3 B 105, 2.4G NFM DPB ANBR ZERENA 3
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199045·AK3 Congruent Insert Trial Size 3, 14mm
Sklar®
FDA UDI
SKLAR CORPORATION·10649111155192·TISSUE FCP 1X2 14"
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973107699·TRIAL 90-SRK-191314 POLY-MPCS 3X14 RIGHT
ADVANIX BILIARY STENT WITH NAVIFLEX RX DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MORPHEUS OX
FDA 510(k)
FDA Class 2
·Anesthesiology
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024
ADVANIX BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 30, 2024
ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 14, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·July 28, 2011
3 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 26, 2008
ADVANIX? BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·October 30, 2025
11.0MM TI HELICAL BLADE 100MM
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·February 3, 2020
ARCHITECT B12 REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CDD·April 17, 2025
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 21, 2025
ALINITY I B12 REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CDD·January 27, 2025
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·February 4, 2025
ALINITY I B12 REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CDD·September 22, 2025