63 results · 22ms · Sources: EU EUDAMED, US FDA

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DynoSense Vital Sign Measuring System

FDA 510(k)
FDA Class 2 ·Cardiovascular

Jawz Endomyocardial Biopsy Forcep

FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333206858·Jawz Endomyocardial Biopsy Forceps 5F x 50cm St...

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690127321·Apex Revision Knee System-Revision Femur Instru...

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668101056·KNAPP RETRACTOR 4-PRONG BLUNT

KMI IMI GROUP

FDA UDI
Innovative Med·00851314007021·Aspiration Cannula

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889981169534·CORTICAL SHANK, Cannulated, 9.0 X 90

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889987169538·CORTICAL SHANK, Cannulated, 9.0 X 90

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690194934·Apex Revision Knee System-Revision Femur Instru...

Coral

FDA UDI
Seaspine Orthopedics Corporation·10889981029111·Prebent Rod 5.5 x 90

AFX INTRODUCER SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

IMPLANTABLE CLIP

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

REZUM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

REZUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

SUPRAMID BLACK 5/0 (1) 45CM DS16

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·January 17, 2019

AFFINITY DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 11, 2014

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013