Hh Global Technology, Inc. is one of 16117 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hh Global Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII), Pen Needle
2
Total
2
Cleared
0
Denied
Hh Global Technology, Inc. has 2 FDA 510(k) cleared medical devices. Based in Buford, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hh Global Technology, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Oconnell Regulatory Consultants, Inc. and Tianjin Huahong Technology Co., Ltd..
FDA 510(k) Regulatory Record - Hh Global Technology, Inc.
2 devices