Tianjin Huahong Technology Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Tianjin Huahong Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Safety lancet (XL), Lancing device, Huahong Sharps Container (HHR-I, HHR-II)
15
Total
15
Cleared
0
Denied
Tianjin Huahong Technology Co., Ltd. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Tianjin, CN.
Latest FDA clearance: Sep 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.
FDA 510(k) Regulatory Record - Tianjin Huahong Technology Co., Ltd.
15 devices
Cleared
Sep 13, 2026
Safety lancet (XL)
General & Plastic Surgery
53d
Cleared
Aug 18, 2026
Lancing device
General & Plastic Surgery
54d
Cleared
Aug 05, 2026
Huahong Sharps Container (HHR-I, HHR-II)
General Hospital
142d
Cleared
Jul 22, 2026
Lancet
General & Plastic Surgery
22d
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