27 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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