12 results
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19ms
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Sources: EU EUDAMED, US FDA
LANTOS 3D EAR SCANNER
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
Z Liquid HT C4-S 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121326·Dental porcelain/ceramic restoration kit
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197527194·Super-Cut Kaye Facelift Scissors
straig...
VIDAS TESTOSTERONE (TES), MODEL 30 418
FDA 510(k)
FDA Class 1
·Clinical Chemistry
NMI IC
FDA 510(k)
FDA Class 2
·General Hospital
COOK CELECT® PLATINUM NAVALIGN JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·June 6, 2011
ALARIS INFUSION SYSTEM
FDA Adverse Event
Other
·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·August 13, 2008
UNK - CONSTRUCTS: LCP
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·May 11, 2026
INSTINCT PLUS ENDOSCOPIC CLIPPING DEVICE
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code PKL·September 29, 2023
SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781260
FDA Enforcement
Class II
·Completed·Philips North America Llc·September 15, 2021