9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EndoEssentials™ Absorbent Paper Points 200 - ISO#25-.02 Taper
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172015035·Endodontic paper point
LINK ACETABULAR MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RAAF DUAL LUMEN CATH. REPAIR KIT 2.2
FDA 510(k)
FDA Class 2
·General Hospital
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·June 25, 2019
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 10, 2014
EASYTRAK 2
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·October 11, 2010
GLOBAL AP 135 DEG TAPER ASSEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWS·December 10, 2012
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021