16 results · 22ms · 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.

EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450139370·

SYNTHES (USA) LARGE FRAGMENT LOCKING COMPRESSION PLATE (LCP) SYSTEM-T PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

TRI-FIX SPINAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 3, 2025

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2014

TOTAL ASR FEM IMP SIZE 51

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 10, 2013

RIATA ST OPTIM ACTIVE-FIXATION LEAD

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

VITALITY 2

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 12, 2011

HEADBAND HB-7 FOR TDH39

FDA Adverse Event
Malfunction ·NATUS MEDICAL DENMARK·Product code EWO·September 17, 2020

HEADBAND HB-7 FOR TDH39

FDA Adverse Event
Malfunction ·NATUS MEDICAL DENMARK APS·Product code EWO·January 12, 2022

HEADSET HB-7 (12 KHZ) MATCHED TDH39 PHONES (JACK)

FDA Adverse Event
Malfunction ·NATUS MEDICAL DENMARK APS·Product code EWO·April 22, 2022