85 results · 22ms · Sources: EU EUDAMED, 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