Trudell Medical International is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Trudell Medical International - FDA 510(k) Cleared Devices
Recent clearances: AeroChamber2go Anti-Static Valved Holding Chamber, Corrugated tube with mouthpiece accessory, AeroEclipse* ONE BAN
9
Total
9
Cleared
0
Denied
Trudell Medical International has 9 FDA 510(k) cleared medical devices. Based in London, CA.
Latest FDA clearance: Jan 2025. Active since 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Trudell Medical International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trudell Medical International
9 devices
Cleared
Jan 15, 2025
AeroChamber2go Anti-Static Valved Holding Chamber
Anesthesiology
132d
Cleared
Jun 14, 2021
Corrugated tube with mouthpiece accessory
Anesthesiology
207d
Cleared
Jul 17, 2020
AeroEclipse* ONE BAN
Anesthesiology
186d
Cleared
Aug 16, 2019
Combined Aerobika OPEP and VersaPAP device
Anesthesiology
281d
Cleared
Jan 11, 2019
AeroChamber Plus* Flow-Vu* Anti-Static Valved Holding Chamber (VHC)
Anesthesiology
203d
Cleared
Aug 17, 2018
VersaPAP Positive Airway Pressure (PAP) Device
Anesthesiology
238d
Cleared
May 02, 2018
MC 300R* Nebulizer
Anesthesiology
135d
Cleared
Feb 28, 2018
MC 300* Nebulizer
Anesthesiology
125d
Cleared
Oct 15, 2015
Aerobika OPEP Devive with Manometer
Anesthesiology
262d