45 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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