42 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PowerPAK Syringe

FDA 510(k)
FDA Class 2 ·General Hospital

HeyGears

FDA UDI
Keystone Industries·H66842201141·KeySplint Hard for HeyGears, 1 kg

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220114150·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220114070·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220114000·

3D KNEE

FDA 510(k)
FDA Class 2 ·Orthopedic

Astroglide Organix Liquid

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

Widex

FDA UDI
Widex A/S·05706069914665·WIDEX MOMENT MRB2D (Honey blond ) 220, Telecoil...

ONE TOUCH BASIC ENHANCED

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·February 26, 2002

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025

VERSACROSS CONNECT LAAC ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 12, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 26, 2024