8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUINTON INJECTION SEALING CAP
FDA 510(k)
FDA Class 2
·General Hospital
JAKOBI SURG. INSTRUMENTS #2 70/71
FDA 510(k)
FDA Class 2
·General Hospital
EMIT QST AMIKACIN ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
FREESTYLE LITE
FDA Adverse Event
Injury
·Product code NBW·June 2, 2014
BV300 9"
FDA Adverse Event
Injury
·PHILIPS HEALTHCARE·Product code OXO·June 15, 2015
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS - INNOVATION CTR - SILICON VALLEY·Product code GEX·September 13, 2010
INSERTER/EXTRACTOR FOR TFN FEMORAL NECK
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HSB·December 8, 2025
PKG, ENDO METZENBAUM SCISSORS, CURVED, P/N 0250080267. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.
FDA Enforcement
Class II
·Terminated·Stryker Endoscopy·December 24, 2014