7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
BACT/ALERT PF
FDA 510(k)
FDA Class 1
·Microbiology
Straumann Screw-Retained Abutments
FDA 510(k)
FDA Class 2
·Dental
SINEXUS SINUS STENT GEN 2, MODEL 1999-25
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
*
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code DRS·February 27, 2013
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
3.5MM TI CORTEX SCREW SELF-TAPPING 55MM
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·December 3, 2020