9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPE
FDA 510(k)
FDA Class 2
·Ophthalmic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756120364·STANDARD BASIN SET
AVR Super-Slide Retractor Frame
FDA UDI
KOROS U.S.A., INC.·10840199538345·AVR Super-Slide Retractor Frame
QUANTIMETRIC PLUS IGM REAGENT KIT
FDA 510(k)
FDA Class 2
·Immunology
CHESEBROUGH-POND'S URI-DRAIN MALE URINARY POUCH
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·June 25, 2014
PINNACLE MTL INS NEUT28IDX44OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 3, 2013
RX ACCULINK CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·November 5, 2010
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020