8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
I.V.E. REFRACTION SYSTEM
FDA 510(k)
FDA Class 1
·Ophthalmic
Preat
FDA UDI
Preat Corporation·00842092140369·Sphero Block Abutment Astra EV 3.0 x 6mm (2.5mm...
ERA® Implant Abutment Micro Ang. Base, 5mm Cuff (D)
FDA UDI
STERNGOLD DENTAL LLC·00841549105661·Implant retained overdentures are an establishe...
ARRW EVOLUTION
FDA 510(k)
FDA Class 2
·General Hospital
STERILE POWDERED LATEX SURGICAL GLOVES WITH PROTEIN LABELING CLAIM (200 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SETROX S 45
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·May 15, 2014
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·August 16, 2010