80 results · 17ms · Sources: EU EUDAMED, US FDA

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INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.

FDA Recall
Open, Classified ·Integra LifeSciences Corp. (NeuroSciences)·Product code KTI·April 4, 2025

binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and Neisseria gonorrhoeae Ref: 1.002.101

FDA Recall
Open, Classified ·Binx Health, Inc. 245 1st St Ste 18 Riverview II Cambridge MA 02142-1292·Product code QEP·March 29, 2023

Beijing Syntech Laser APOLLO V+ Medical Platform surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser UL Station surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser Nice Station Light Based Platform surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser Trixel 11 C02 Laser surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser UL C02 Laser surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser Diode Laser surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser Trixel C02 Laser surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers

FDA Recall
Open, Classified ·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017

MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.

FDA Recall
Open, Classified ·Integra LifeSciences Corp. (NeuroSciences)·Product code FMF·May 23, 2025

CereLink ICP Monitor; Catalog No. 826820, 826820P. Intracranial pressure monitor.

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code GWM·June 22, 2022

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

FDA Recall
Open, Classified ·LivaNova USA Inc·Product code LYJ·November 16, 2018

BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units

FDA Recall
Open, Classified ·CareFusion 303, Inc.·Product code FRN·May 21, 2024

CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821749

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code JXG·May 7, 2024

CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821750

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code JXG·May 7, 2024

CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821745

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code JXG·May 7, 2024

Permobil TiLite, Models: Aero Z, and ZRA

FDA Recall
Open, Classified ·TiSport, Llc·Product code IOR·September 24, 2021

Ref No: HITHSP04 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code HBG·January 19, 2024

Ref No: HITHSP06 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.

FDA Recall
Open, Classified ·Integra LifeSciences Corp.·Product code HBG·January 19, 2024