10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
OCU-1
FDA 510(k)
FDA Class 1
·Ophthalmic
Centerline Cannulated Accessories
FDA UDI
Life Spine, Inc.·00190837021061·
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809916493249·Multi-Axial Fenestrated Screw, Ø5.0 x 30mm, Ø6....
Arthrex®
FDA UDI
ARTHREX, INC.·00888867523913·Spine Compression Screw, 5.0x30mm
CHAMPY BONE PLATES & BONE SCREWS
FDA 510(k)
FDA Class 2
·Dental
CRONEX SR342-QUANTA FAST DETAIL-INTENSI-SCREENS
FDA 510(k)
FDA Class 1
·Radiology
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code GZB·June 16, 2014
CAPSUREFIX
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·December 17, 2012
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021