8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
ACROMED BONE SCREW TAP SLEEVES
FDA 510(k)
FDA Class 1
·Orthopedic
GC Initial™
FDA UDI
Gc America Inc.·J0228730671·GC Initial™ AL Enamel E-57, 20g
ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS
FDA 510(k)
FDA Class 2
·Dental
LightForce LTS Model 1000, 1500, 2500, and 4000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COBAS 8000 COBAS C 502 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·March 26, 2026
LIGACLIP MCA APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDO·June 13, 2014
PUMP MMT-522NAS PRDGM INS V2.2 SK EN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 15, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·December 13, 2012