9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
EMIT D.A.U. PROPOXYPHENE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Clamp
FDA UDI
KOROS U.S.A., INC.·10840199535894·Cooley Angeld Clamp w/ Serrated 12mm Jaw, 17.5...
truFreeze System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CZR PRESS LF STAINS
FDA 510(k)
FDA Class 2
·Dental
COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING ARCOM XL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PAO·November 9, 2017
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·February 12, 2014
SYNREAM REAMER HEAD Ø12.5
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTO·November 29, 2012
UNKNOWN DEPUY LCS LG 10MM MEDIAL LEFT 10MM MENISCAL BEARING
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code NJL·September 29, 2010
XP-XP Tibial Tray - Interlok 69 mm Item # 195754
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019