60 results · 28ms · Sources: EU EUDAMED, US FDA

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CALIBRATING MATERIAL, BUFFERS, STANDARD

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

OCTAGON BL NC Abutment 0° Ø 3.5 mm, L 5.5 mm GH 1.0 mm, cementable basic screw 2

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50220271·BL NC Abutment 0° Ø 3.5 mm, L 5.5 mm GH 1.0 mm,...

Safco polycarbonate crowns

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310220273·Safco polycar crwn ant/bicspd 120crwn

AOS CANCELLOUS SCREW 5.0mm x 27.5mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019988·

MODIFICATION TO XIA SPINE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

FOCUS RADIATION TREATMENT PLANNING SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

BOSTON SCIENTIFIC BILIARY STENT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PNB·December 3, 2025

LOW SORBING SECONDARY SET SMARTSITE NEEDLE-FREE VALVE BAG ACCESS

FDA Adverse Event
Malfunction ·BD SWITZERLAND SARL·Product code LHI·March 25, 2026

LOW SORBING SECONDARY SET SMARTSITE NEEDLE-FREE VALVE BAG ACCESS

FDA Adverse Event
Malfunction ·BD SWITZERLAND SARL·Product code LHI·March 25, 2026

MARQUEE

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·August 9, 2024

PHASEAL CONNECTORS

FDA Adverse Event
Malfunction ·UNKNOWN·Product code ONB·May 7, 2026

DOSI FUSER ELASTOMERIC PUMP (250D2 TYPE); PHASEAL CONNECTORS

FDA Adverse Event
Malfunction ·EPIC INTERNATIONAL (THAILAND) CO., LTD.·Product code MEB·May 7, 2026

ROTAREX

FDA Adverse Event
Malfunction ·STRAUB MEDICAL AG·Product code MCW·August 28, 2024

PTFE FELT PLEDGETS

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DXZ·March 2, 2023

OT VERIO IQ METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·March 10, 2011

DTC MARGRON HIP REPLACEMENT SYSTEM

FDA Adverse Event
Injury ·PORTLAND ORTHOPAEDICS LTD.·Product code LPH·April 1, 2008

25GX1IN HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·June 15, 2023

PEN NEEDLE AUTOSHIELD DUO 30GX5MM EU

FDA Adverse Event
Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·November 12, 2024

DENALI JUGULAR SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 30, 2024