Venner Medical (Singapore) Pte, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venner Medical (Singapore) Pte, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Venner PneuX™ TT (Tracheostomy Tube) Size 7.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 8.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 9.0 mm, Venner PneuX™ ETT (Endotracheal Tube) 6 mm, Venner PneuX™ ETT (Endotracheal Tube) 7 mm, Venner PneuX™ ETT (Endotracheal Tube) 8 mm, Venner PneuX™ ETT (Endotracheal Tube) 9 mm, APA Oxy Blade
Venner Medical (Singapore) Pte, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 6 cleared submissions from 2010 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Venner Medical (Singapore) Pte, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Brauer Device Consultants, LLC as regulatory consultant.