35 results · 54ms · Sources: EU EUDAMED, US FDA

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ASPIRE PRODUCTS, LLC

FDA registration
ASPIRE PRODUCTS, LLC·2 products·🇺🇸 United States

EMST150

FDA UDI
Aspire Products LLC·00793573085498·EMST150 expiratory muscle strength trainer (han...

EMST150 EXPIRATORY MUSCLE STRENGTH TRAINER

FDA Adverse Event
Injury ·ASPIRE PRODUCTS, LLC·Product code ION·September 3, 2024

BALLARD CLOSED SUCTION CATHETER, Y-ADAPTER, NEONATAL/PEDIATRIC

FDA Adverse Event
Malfunction ·AVENT S DE RL DE CV·Product code BSY·February 7, 2025

BALLARD CLOSED SUCTION SYSTEM

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BSY·February 13, 2025

BALLARD CLOSED SUCTION SYSTEM FOR ADULTS

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BSY·January 30, 2025

NEXUS® SONASTAR® SHORT HANDPIECE

FDA Adverse Event
Injury ·MISONIX, INC.·Product code LFL·May 3, 2024

BONESCALPEL® ULTRASONIC SURGICAL ASPIRATION SYSTEM

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·April 6, 2023

BALLARD CLOSED SUCTION CATHETER, Y-ADAPTER, NEONATAL/PEDIATRIC

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BSY·February 11, 2025

NEXUS® SONASTAR ELITE HANDPIECE

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·October 3, 2024

SONASTAR® ULTRASONIC SURGICAL ASPIRATION SYSTEM

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·December 23, 2022

NEXUS® STANDARD HANDPIECE

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·May 10, 2023

NEXUS® STANDARD HANDPIECE

FDA Adverse Event
Injury ·MISONIX, INC.·Product code LFL·July 18, 2023

SONASTAR® STANDARD LONG CURVED PROBE

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·March 21, 2024

NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·December 6, 2023

NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM

FDA Adverse Event
Malfunction ·MISONIX, INC.·Product code LFL·December 6, 2023

Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspirate saliva, mucous, vomitus or other aspirant from the mouth or airway to allow adequate respiration or ventilation of the patient.

FDA Recall
Terminated ·Ohio Medical Corporation·Product code BTA·August 14, 2018

VIZIGO¿ SHEATH

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·July 10, 2024

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code LHI·September 13, 2021

CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ SMALL

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·June 19, 2024