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

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MYOSURE XL ROD LENS HYSTEROSCOPE, MYOSURE XL OUTLFOW CHANNEL

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

HYDROCEL VERTEBRAL BODY REPLACEMENT, MODEL 06-172-00XX1

FDA 510(k)
FDA Class 2 ·Orthopedic

SINGLE CANNULA EXTENDED APPLICATOR

FDA 510(k)
FDA Class 1 ·General Hospital

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 13, 2024

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 27, 2024

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 15, 2023

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·November 28, 2023

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 27, 2025

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 6, 2023

EQ REV COMPRESS SCREW LCK CAP KIT, 4.5 X 26MM

FDA Adverse Event
Malfunction ·EXACTECH, INC.·Product code KWT·October 6, 2022

OLYMPUS ELECTROSURGICAL UNIT

FDA Adverse Event
Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·May 17, 2013

ENRHYTHM DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 14, 2011

*

FDA Adverse Event
Injury ·ALBAHEALTH LLC DIV·Product code GAD·August 14, 2008

BD KIESTRA IDENTIFA

FDA Adverse Event
Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

BD KIESTRA¿ IDENTIFA

FDA Adverse Event
Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·December 9, 2024