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

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MiniCAT 2D

FDA 510(k)
FDA Class 2 ·Radiology

NA

FDA UDI
Control Devices, LLC·G29820182508·The CGA 870 regulator is designed for use with ...

CODMAN

FDA UDI
Cerenovus, Inc.·10886704002246·CODMAN Slimline Mini Aneurysm Clip No 6 Straigh...

Conventional Lead Apron .5mm Medium 24 X 39

FDA UDI
Flow X Ray Corporation·00843696123284·Conventional Lead Apron .5mm Medium 24 X 39, Black

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981309770·Trial Rasp, 31mm x 24mm x 18mm, 25 Deg

3D Printed Interbody Systems

FDA UDI
Seaspine Orthopedics Corporation·10889981303884·2-Hole No-Profile Interbody, 31mm x 24mm x 18mm...

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981215293·No-Profile Interbody, 31mm x 24mm x 18mm, 25 deg

Control Devices

FDA UDI
Control Devices, LLC·00810051631814·CGA 870 Oxygen Regulator, 50 psig, Barbed Outle...

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383549363·"An absorbent paper points is an endodontic pap...

STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER

FDA 510(k)
FDA Class 2 ·Radiology

MODIFICATION TO SPIRAL RADIUS 90-D SST SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

APPLE ECG (ELECTROCARDIOGRAPH) APP

FDA Adverse Event
Injury ·APPLE INC.·Product code QDA·July 5, 2023

TABLE, VTS, 120VAC

FDA UDI
The Wells Johnson Company·B458201825000·TABLE, VTS (VIBRATORY TISSUE SEPARATOR/SHAKER),...

Widex

FDA UDI
Widex A/S·05706069728118·Widex EVOKE E-FS (Cappuccino brown S-440 ) Tele...

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 14, 2018

U BY KOTEX SLEEK

FDA Adverse Event
Malfunction ·KIMBERLY-CLARK CORPORATION·Product code HEB·August 14, 2018

AXIOM PX IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·December 3, 2018

HANDICARE STAIRLIFTS 2000

FDA Adverse Event
Malfunction ·HANDICARE ACCESSIBILITY UK LTD·Product code PCD·February 5, 2019

AXIOM REG IMPLANT

FDA Adverse Event
Injury ·ANTHOGYR·Product code DZE·July 26, 2019