23 results · 23ms · Sources: EU EUDAMED, 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