15 results
·
29ms
·
Sources: EU EUDAMED, US FDA
GDT-1000 System
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MAESTRO TOTAL WRIST
FDA UDI
Biomet Orthopedics, LLC·00880304269118·
Maestro™ Total Wrist
FDA UDI
Biomet Orthopedics, LLC·00887868239403·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694014953·1.6mm Low Profile, X-Large Bur Hole Plate
OsteoMed
FDA UDI
OSTEOMED LLC·00845694065580·1.6 System Low Profile X-Large Bur Hole Plate S...
LINAC COLLIMATOR ASSEMBLY HOUSING (LCAH) MODEL LCAHART
FDA 510(k)
FDA Class 2
·Radiology
MULTIFIX P KNOTLESS FIXATION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
RD SET YI
FDA Adverse Event
Malfunction
·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021
RD SET DCI
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023
NOVOSTITCH PRO MENISCAL REPAIR SYSTEM, SIZE 2-0
FDA Adverse Event
Malfunction
·CETERIX ORTHOPAEDICS·Product code GAT·February 14, 2019
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·June 20, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·July 27, 2011
XIA 3 TITANIUM POLYAXIAL SCREW DIA 6.5 X 60 MM
FDA Adverse Event
Injury
·STRYKER SPINE BORDEAUX·Product code KWP·September 29, 2008
RD SET
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code DQA·December 31, 2025
RD SET
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code DQA·December 31, 2025