247 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HARDYDISK, NALIDIXIC ACID, 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
TruFlex™
FDA UDI
Ortho Organizers, Inc.·00190707127305·Truflex™ PT SE NiTi Upper 17x25 38mm (10PK)
BIO2 TECHNOLOGIES
FDA UDI
BIO2 TECHNOLOGIES, INC.·B01010001301·Vitrium PIP Standard Angled
TruFlex
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730011855·Truflex™ PT SE NiTi Upper 17x25 38mm 10/PK
Responsive Respiratory, Inc.
FDA UDI
RESPONSIVE RESPIRATORY, INC.·00851440007490·Swivel Hose Nipple, Barb 25/pack
eWave 6-Lead EKG
FDA UDI
Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...
Lattus
FDA UDI
Seaspine Orthopedics Corporation·10889981307608·Posterior Blade, SS, 130mm
CURE ACP
FDA UDI
SpineArt SA·07640270064291·ANTERIOR CERVICAL PLATE, 1 LEVEL L30
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132119440·ø3.0mm Flexible IM Nail Cap (2 Each)
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167900001300·
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520001300·Curved Titanium Rod
TAURUS
FDA UDI
CTL Medical Corporation·00841732150799·5.5mm Curved Rod 130mm Ti Alloy
Lattus
FDA UDI
Seaspine Orthopedics Corporation·10889981307707·Cephalad/Caudal 130mm Blade, AL
CarboJet® CO2 Bone Lavage System
FDA UDI
Kinamed, Inc.·00818720012391·CO2 Pressure Regulator with DIN 6 Connector
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700001300·
Preference 2
FDA UDI
SINTX Technologies, Inc.·M555102000130·Curved Rod 6.0mm, 130mm
Taurus Pedicle Screw System
FDA UDI
SINTX Technologies, Inc.·M555252000130·Taurus Pedicle Screw System-Curved Rod 5.5x130mm
CAMLOG ROOTFORM IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
6000130-2006-00045
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQX·March 10, 2006