15 results
·
33ms
·
Sources: EU EUDAMED, US FDA
QUALTEX SKIN STAPLE EXTRACTOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PAQ.112X100X300/QI-HS/GOLDWAY
FDA UDI
AB MEDICA GROUP, S.A.·08428763008637·
Couture Essence
FDA UDI
Carolon Company·00078301971244·
Couture Essence
FDA UDI
Carolon Company·00078301911240·
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756020268·FINGER SPLINT
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G5869112040·round caps, gas or steam permeable, can be used...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112040·Tap, 6.5 mm
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0112040·Tap, 5.50mm
CELL-DYN 22 PLUS CALIBRATOR
FDA 510(k)
FDA Class 2
·Hematology
NEUROFAX, MODELS EEG-1100A, EEG-9100A
FDA 510(k)
FDA Class 2
·Neurology
MICROCLAVE® CLEAR CONNECTOR
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·November 12, 2019
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 30, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 2, 2014
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026