111 results · 31ms · Sources: EU EUDAMED, US FDA

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GS MEDICAL ANYPLUS PEEK LUMBAR CAGES (ALIF AND DLIF)

FDA 510(k)
FDA Class 2 ·Orthopedic

Depth gauge

FDA UDI
Jeil Medical Corporation·08800089407736·

5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/65MM

FDA Adverse Event
Injury ·SYNTHES MEZZOVICO·Product code JDP·August 28, 2015

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·January 26, 2015

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·March 2, 2015

HIGH TIBIAL OSTEOTOMY PLATING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

FETCH 2 ASPIRATION CATHETER MODEL 109400-001

FDA 510(k)
FDA Class 2 ·Cardiovascular

IMPLANT, FIXATION DEVICE CONDYLAR PLATE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code JDP·February 23, 2017

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·Product code NJK·June 28, 2021

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·Product code NJK·June 28, 2021

VALVE IN CARTRIDGE, 7MM

FDA Adverse Event
Injury ·Product code NJK·June 28, 2021

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·GYRUS ACMI, INC·Product code NJK·May 21, 2022

VALVE IN CARTRIDGE, 7MM

FDA Adverse Event
Injury ·GYRUS ACMI, INC·Product code NJK·May 21, 2022

VALVE IN CARTRIDGE, 6MM

FDA Adverse Event
Injury ·GYRUS ACMI, INC.·Product code NJK·March 13, 2023

VALVE IN CARTRIDGE, 7MM

FDA Adverse Event
Injury ·GYRUS ACMI, INC.·Product code NJK·July 26, 2024

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·GYRUS ACMI, INC.·Product code NJK·July 16, 2024

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·Product code NJK·July 15, 2020

VALVE IN CARTRIDGE, 9MM

FDA Adverse Event
Injury ·Product code NJK·July 15, 2020

VALVE IN CARTRIDGE, 5MM

FDA Adverse Event
Injury ·Product code NJK·July 10, 2020

VALVE IN CARTRIDGE, 7MM

FDA Adverse Event
Injury ·Product code NJK·July 10, 2020