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

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THE ADVANCE CATHETER FOR HSG AND SIS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ArgenPMMA 95x30-B4

FDA UDI
ARGEN CORPORATION, THE·D818123258·Crown And Bridge, Temporary, Resin

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970584·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970591·

DUET TRS RELOADS, DUET TRS RELOADS WITH TRI-STAPLE TECHNOLOGY, ENDO GIA UNIVERSAL AND ULTRA UNIVERSAL STAPLERS

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

NOVEON

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

IMP TM 4.7MM MTX FULL, 11.5MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·June 27, 2024

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
UNKNOWN·Product code ITJ·May 21, 2013

UNKNOWN_RECONSTRUCTIVE_PRODUCT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 26, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 14, 2011

IMP TM 4.7MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·October 30, 2024

IMP TM 6.0MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·June 29, 2023

HEMOCONCENTRATOR BC 20 PLUS

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KDI·April 1, 2016

TRI-LOCK BPS SZ 4 HI OFFSET

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 26, 2020

Quadra Assura, Sterile EO, Model #/ Part #: CD3265-40/100042335, 100059846; CD3265-40Q/100042336, 100059847; CD3267-40/100042956, 100043569, 100059961, 100078810; CD3267-40Q/100043132, 100043539, 100059917, 100059956, 100078904; CD3365-40C/100080435, 100080436; CD3365-40Q/100080426, 100080427; CD3367-40/100078813, 100079497, 100096097; CD3367-40C/100078597, 100079174, 100079450, 100079490, 100105524; CD3367-40Q/100078851, 100079212, 100079504, 100096098; CD3367-40QC/100078656, 100079193, 100079498, 100079524, 100105513, 100105514, 100138185, 100138213; CD3385-40C/100080778; CD3385-40QC/100080780, 100105489

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018