27 results · 25ms · Sources: EU EUDAMED, US FDA

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Daily Breeze B (olifilcon B) Spherical Silicone Hydrogel Soft Contact Lens, Daily Breeze B (olifilcon B) Toric Silicone Hydrogel Soft Contact Lens, Daily Breeze B (olifilcon B) Multifocal Silicone Hydrogel Soft Contact Lens

FDA 510(k)
FDA Class 2 ·Ophthalmic

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112656·BARRON CORNEAL PUNCH 8.5MM

Ophthlamic Speculum

FDA UDI
KATENA PRODUCTS, INC.·10841668112424·DISPOSABLE BARRAQUER SPECULUM BOX OF 10

Preference

FDA UDI
CTL Medical Corporation·00841732152069·7.2mm Polyaxial Screw Reduction 80mm Green

Viceroy

FDA UDI
DIOMEDICAL CO.,LTD.·08800113905030·VICEROY Rod - 6.0 (D)6x(L)80mm

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·July 17, 2020

SPINE SYSTEM EVOLUTION

FDA 510(k)
FDA Class 2 ·Orthopedic

NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS

FDA 510(k)
FDA Class 2 ·General Hospital

Trilogy® Trabecular Metal™

FDA UDI
Zimmer, Inc.·00889024118645·

I-STAT 6+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·September 28, 2021

HEARTWARE® VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Malfunction ·HEARTWARE, INC·Product code DSQ·October 27, 2014

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·August 11, 2011

PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC.·Product code NBW·January 28, 2011

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR - CARDIAC THERAPIES·Product code NIQ·September 24, 2010

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·September 24, 2010

ON-X AORTIC HEART VALVE WITH ANATOMICAL SEWING RING AND EXTENDED HOLDER

FDA Adverse Event
Death ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·February 2, 2017

ON-X ASCENDING AORTIC PROSTHESIS

FDA Adverse Event
Death ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·February 8, 2017

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR - CARDIAC THERAPIES·Product code NIQ·September 24, 2010

SYNVISC ONE (HYLAN G-F 20) INJECTION

FDA Adverse Event
Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·September 21, 2010