19 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Klassic HD Hip System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741514400·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674151440060·
LoFric® Primo™
FDA UDI
Wellspect AB·07392532131608·Single Use Urinary Catheter LoFric Primo Coudé ...
LoFric® Primo™
FDA UDI
Wellspect AB·07333387043197·Single Use Urinary Catheter LoFric Primo Coudé ...
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837087784·
MAYFIELD INFINITY SKULL CLAMP
FDA 510(k)
FDA Class 2
·Neurology
GMD UNIVERSAL URINARY INCONTINENCE SLING, MODEL 1012
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VERSYS FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER INC·Product code LPH·February 25, 2016
VC10 PUMP, 115V
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code HHK·January 2, 2025
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code DTK·June 7, 2013
ISYMM ASPHERIC INTRAOCULAR LENS
FDA Adverse Event
Malfunction
·HOYA SURGICAL OPTICS, INC.·Product code HQL·June 21, 2011
CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·September 5, 2008
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
FDA Enforcement
Class II
·Terminated·Cardiovascular Systems Inc·May 31, 2017
Medical Linear Accelerator
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·September 14, 2016