23 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
Stryker GmbH·00886385005683·Cortical Screw, Self-tap., T10 Drive
SureLOK Mini Posterior Cervical/Upper Thoracic System
FDA UDI
PRECISION SPINE, INC.·00840019907118·3.5mm x 20mm SureLOK™ PC Screw
Symmetry Metzenbaum
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482051566·Symmetry® Scissors, Metzenbaum Dissecting, Curv...
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0430200·Sagittal Bender, Double Ended Left
NEXAN SYSTEM, MODEL NX-300
FDA 510(k)
FDA Class 2
·Cardiovascular
BLUEPHASE
FDA 510(k)
FDA Class 2
·Dental
HNM Medical
FDA UDI
HNM STAINLESS, LLC.·00842962107669·METZENBAUM SCISSORS, 8", SLIM DELICATE, CVD
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
SECURE 3 MED/SURG BEDOBS 01/13
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 9, 2013
ISYMM ASPHERIC INTRAOCULAR LENS
FDA Adverse Event
Malfunction
·HOYA SURGICAL OPTICS, INC.·Product code HQL·February 25, 2011
VITALITY DS
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERSA-DIAL 42X18X46 HUM HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSD·November 19, 2021