14 results · 21ms · 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.

STRAUMANN CARES BONE LEVEL SCREW RETAINED BARS, STRAUMANN CARES BONE LEVEL SCREW RETAINED BRIDGES

FDA 510(k)
FDA Class 2 ·Dental

LIAISON 25 OH VITAMIN D

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ALL-BOUND 3

FDA 510(k)
FDA Class 2 ·Dental

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
Malfunction ·INVAMEX·Product code ILS·October 1, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 29, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 17, 2011

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

PEDICLE SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

PEDICLE SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

INSPIRE HVR DUAL

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTN·November 12, 2024

INSPIRE HVR DUAL HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

FDA Adverse Event
Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·November 18, 2022

Achieva 1.5T

FDA Enforcement
Class II ·Ongoing·Philips North America Llc·November 29, 2023