7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
BECTON DICKINSON ARTERIAL BLOOD GAS KITS
FDA 510(k)
FDA Class 2
·General Hospital
LUMENIS FAMILY OF IPL SYSTEMS AND COMBINATION IPL/ND:YAG SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SAUFLON CLARITI (SOMOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER
FDA 510(k)
FDA Class 2
·Ophthalmic
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEA·Product code BTR·January 22, 2013
PENUMBRA SYSTEM SEPARATOR 032
FDA Adverse Event
Malfunction
·PENUMBRA INC.·Product code NRY·November 18, 2010
3.7MM TI CERVICAL SPINE SCREW SLF-DRLG/VARIABLE ANGLE 16MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code OVE·July 11, 2014
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm Catalog Number: 18965045S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Enforcement
Class II
·Terminated·Stryker GmbH·June 24, 2020