Vitaltec Corporation is one of 453 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Vitaltec Corporation - FDA 510(k) Cleared Devices
Recent clearances: Venti-Trach Tracheostomy Tube (570 Series), 5300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm, ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH
3
Total
3
Cleared
0
Denied
Vitaltec Corporation has 3 FDA 510(k) cleared medical devices. Based in Hsin Chu City, TW.
Latest FDA clearance: Sep 2026. Active since 2010. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vitaltec Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ruscert Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Vitaltec Corporation
3 devices