18 results · 22ms · Sources: EU EUDAMED, US FDA

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DEMETECH POLYDIOXANONE SYNTHETIC MONOFILAMENT (PDO) ABSORBABLE SUTURE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·June 11, 2024

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·July 3, 2024

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·May 9, 2024

DEMEDIOX

FDA Adverse Event
Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

THERMIQUE

FDA 510(k)
FDA Class 2 ·Dental

VORTEX

FDA 510(k)
FDA Class 2 ·Radiology

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code FRO·February 14, 2023

QUIK-COMBO PACING/DEFIBRILLATION/ECG

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code FRO·October 12, 2022

UNKNOWN_RECONSTRUCTIVE_PRODUCT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·April 29, 2013

55MM NTLC SELECTABLE RELOAD

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 9, 2011

SPACEMAKER BLUNT TIP TROCAR 10MM

FDA Adverse Event
Malfunction ·PONCE - USS·Product code GCJ·July 25, 2008

CELOX GAUZE

FDA Adverse Event
Injury ·MEDTRADE PRODUCTS LIMITED·Product code QSY·June 10, 2025

Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm, Sterile EO, Rx Only, Quantity 1, UDI: 07613327376067

FDA Enforcement
Class II ·Terminated·Stryker Sustainability Solutions·February 3, 2021

On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems, Inc.·April 30, 2014