7 results
·
33ms
·
Sources: EU EUDAMED, US FDA
AIRCO OXYGEN REGULATOR
FDA 510(k)
FDA Class 1
·Anesthesiology
TOPCON MODEL TRC-NW200 NON-MYDRIATIC RETINAL CAMERA
FDA 510(k)
FDA Class 2
·Ophthalmic
LS SERIES LINEAR STAPLER AND RELOADS, CLC SERIES CURVED LINEAR CUTTER AND RELOADS, LC SERIES LINEAR CUTTER AND RELOADS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 30, 2014
LIFESTENT SOLO VASCLUAR STENT SYSTEM
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·October 23, 2012
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·September 22, 2010
TI Single Vector Distractor Body with Left Foot/30mm; Catalog ID 487.965 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular deficiencies or post-traumatic defects.
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·August 24, 2016