85 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AUTO DETECT FOR TELAHEART DR200/E-A
FDA 510(k)
FDA Class 2
·Cardiovascular
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193105031·HA PEEK EVOS Curved, , 14mmx10mmx 26mm , BICONV...
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690132·Advanced Dental Implant Ø5mm L11.5mm
Ormco
FDA UDI
ORMCO CORPORATION·00889989026450·ARCH PREFORMED LOWER 14 DIA. PK/20
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690347·Titanium Straight Abutment Internal Hex. SP Ø5....
Aligned Medical Solutions
FDA UDI
Aligned Medical Solutions·B0980070040·PERI PACK
BARCOMED 5MP1H
FDA 510(k)
FDA Class 2
·Radiology
INSTANT-VIEW METHADONE URINE DIP STRIP TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 28, 2020
DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HTJ·August 14, 2015
DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HTJ·June 12, 2013
DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HTJ·June 12, 2013
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·LIFESTENT FLEXSTAR & FLEXSTAR XL VASCULAR STENT SYSTEM
DEPUY ASR XL FEM IMP SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 22, 2013
VITROS ECI IMMUNODIAGNOSTIC SYSTEM (RECERTIFIELD)_
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·July 2, 2008
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIM·April 26, 2011
DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HTJ·June 12, 2013
SYNERGY II EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 14, 2017
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·LIFE STENT VASCULAR STENT SYSTEM
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·BARD LIFESTENT VASCULAR STENT SYSTEMS