Tianjin Huahong Technology Co., Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Tianjin Huahong Technology Co., Ltd. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Tianjin, CN.
Latest FDA clearance: Feb 2026. Active since 2021.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Landlink Healthcare Technology (Shanghai) Co., Ltd. as regulatory consultant.
11 devices
Cleared
Feb 12, 2026
Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)
General & Plastic Surgery
188d
Cleared
Dec 09, 2025
Lancing device (HH-XV-T)
General & Plastic Surgery
15d
Cleared
Jun 26, 2025
safety lancet
General & Plastic Surgery
24d
Cleared
Nov 15, 2024
Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX)
General & Plastic Surgery
25d
Cleared
Jun 20, 2024
Safety Lancet (XXXV)
General & Plastic Surgery
14d
Cleared
May 21, 2024
Safety lancet (XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV.)
General & Plastic Surgery
57d
Cleared
Jul 06, 2022
Lancet (I, II, III, V, VI)
General & Plastic Surgery
138d
Cleared
Jul 01, 2022
Insulin Pen Needle
General Hospital
67d
Cleared
May 19, 2022
Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)
General & Plastic Surgery
99d
Cleared
May 17, 2022
Heel Stick Safety Lancet (HHZ-II, HHZ-III)
General & Plastic Surgery
97d
Cleared
Nov 12, 2021
Insulin Pen Needle (Ordinary Type), Insulin Pen Needle (Safety Type)
General Hospital
452d