Vyaire Medical, Inc. is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Vyaire Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AirLife™ Open Et Oxygen Mask, AirLife™ Open Et+ Oxygen Mask, AirLife DuoTherm™ Humidification System, LTV2 Series Ventilators
9
Total
9
Cleared
0
Denied
Vyaire Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Helsinki, FI.
Latest FDA clearance: Nov 2024. Active since 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vyaire Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vyaire Medical, Inc.
9 devices
Cleared
Nov 12, 2024
AirLife™ Open Et Oxygen Mask, AirLife™ Open Et+ Oxygen Mask
Anesthesiology
592d
Cleared
Aug 10, 2023
AirLife DuoTherm™ Humidification System
Anesthesiology
90d
Cleared
Nov 10, 2021
LTV2 Series Ventilators
Anesthesiology
566d
Cleared
Aug 16, 2021
Multi-Link X2 ECG Cable and Leadwire System
Cardiovascular
110d
Cleared
Oct 09, 2020
Multi-LinkTM X2 ECG Adapter and Leadwires
Cardiovascular
221d
Cleared
Sep 13, 2019
Multi-Link X2 ECG and SpO2 Adapter
Cardiovascular
123d
Cleared
Aug 16, 2019
Vyntus BODY
Anesthesiology
136d
Cleared
Nov 30, 2018
Vyntus ONE with CART, Vyntus ONE PFT only with CART, Vyntus ONE with...
Anesthesiology
172d
Cleared
Apr 30, 2018
Gas Sampling Line, Coextruded, 2m/7ft, 10/pkg, Disposable/ 100/pkg,...
Anesthesiology
328d