72 results · 20ms · Sources: EU EUDAMED, US FDA

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CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS

FDA 510(k)
FDA Class 2 ·Orthopedic

ArgenZ HT+ 98x16 ML C4B

FDA UDI
ARGEN CORPORATION, THE·D818130343·Dental porcelain/ceramic restoration kit

ABC

FDA UDI
Conmed Corporation·30653405055369·ABC NOZZLE, SINGLE USE NOZZLE

PAP-CAP

FDA 510(k)
FDA Class 2 ·Anesthesiology

DIEGO POWERED DISSECTOR HANDPIECE WITH STARLINK IMAGE-GUIDED ADAPTER MOUNTING INTERFACE

FDA 510(k)
FDA Class 2 ·Neurology

ABC R/U HANDPIECE NOZZLE

FDA Adverse Event
Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code HAM·March 27, 2020

ADVANTA 2 BED

FDA Adverse Event
Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·March 8, 2013

VERSACARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·May 9, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 22, 2008

Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium

FDA Enforcement
Class II ·Terminated·Exactech, Inc.·November 25, 2020

INSPIRE 6F

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·October 28, 2025

RESERVOIR INSPIRE 8

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 8, 2026

ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catalog No. 130343, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.

FDA Recall
Terminated ·ConMed Corporation·Product code HAM·December 27, 2012

ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catalog No. 130343, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.

FDA Enforcement
Class II ·Terminated·ConMed Corporation·January 30, 2013

INSPIRE HVR HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·December 18, 2025

INSPIRE HARD VENOUS RESERVOIR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·July 25, 2022

INSPIRE HVR HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

FDA Adverse Event
Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·January 13, 2023

INSPIRE 8 HOLLOW FIBER OXYGENATOR W/ INTEGRATED HARDSHELL VENOUS/CARDIOTOMY RES

FDA Adverse Event
SORIN GROUP ITALIA S.R.L.·Product code DTZ·December 19, 2016

HISTOACRYL FLEXIBLE PACK 5

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL SA·Product code MPN·February 11, 2020

INSPIRE HVR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·July 21, 2022