38 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.

GR-17 Resin System

FDA 510(k)
FDA Class 2 ·Dental

CODMAN

FDA UDI
Cerenovus, Inc.·10886704002260·CODMAN Slimline Mini Aneurysm Clip No 6 90 Degr...

Procedure Products Needle

FDA UDI
PROCEDURE PRODUCTS, INC.·B1602018271·Potts Needle, 18ga x 7cm

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383549387·"An absorbent paper points is an endodontic pap...

PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325

FDA 510(k)
FDA Class 2 ·General Hospital

MODIFICATION TO ACCU-CHEK ACTIVE SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

AEQUALIS REVERSED II

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·August 21, 2018

Widex

FDA UDI
Widex A/S·05706069720211·Widex D-9 BTE (Winter silver S-220 ) Telecoil, ...

AEQUALIS ASCEND FLEX SHOULDER PROSTHESIS

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·August 21, 2018

RESTORE

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 15, 2018

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 11, 2026

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 1, 2024

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·September 20, 2024

HAHN TAPERED IMPLANT Ø3.5 X 13 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·January 6, 2024

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 19, 2025

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

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

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 6, 2025

HAHN TAPERED IMPLANT Ø3.5 X 10 MM

FDA Adverse Event
Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·January 6, 2025

U BY KOTEX CLICK

FDA Adverse Event
Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·April 13, 2018

HEPARIN FLUSH, HEPARIN FLUSH

FDA Adverse Event
Other ·Product code NZW·October 17, 2008