27 results
·
22ms
·
Sources: EU EUDAMED, US FDA
VARIS 1.4G
FDA 510(k)
FDA Class 2
·Radiology
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00126431·
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00164031·
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001643·artVeneer life upper anteriors, IS, BL4
Scanlan® SURG-I-BAND® color coding
FDA UDI
SCANLAN INTERNATIONAL INC·00846159001402·Scanlan® SURG-I-BAND® color coding - Narrow, Li...
KAWASUMI LABORATORY BLOOD DRAWING KIT
FDA 510(k)
FDA Class 2
·Hematology
INPLANT ORTHODONTIC ANCHOR SYSTEM
FDA 510(k)
FDA Class 2
·Dental
VERTEBRAL BODY SET/SMALL- STERILE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KWQ·August 9, 2021
DRIVER SHAFT, T-15, LONG
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code LXH·September 13, 2018
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·January 16, 2025
DRIVER SHAFT, T-15, LONG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, LONG
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
3.0MM HEX DRIVER
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
DRIVER SHAFT, T-15, MEDIUM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 14, 2021
PERIPHERAL SCREW, NL, UNI REV, 4.5X42MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·June 5, 2019
HEART START XL
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 7, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·February 18, 2011