Tianjin Huahong Technology Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252490Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)February 12, 2026
K253706Lancing device (HH-XV-T)December 9, 2025
K251694safety lancetJune 26, 2025
K243306Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-TNovember 15, 2024
K241627Safety Lancet (XXXV)June 20, 2024
K240806Safety lancet (XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV.)May 21, 2024
K220475Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIIJuly 6, 2022
K221176Insulin Pen NeedleJuly 1, 2022
K220370Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)May 19, 2022
K220372Heel Stick Safety Lancet (HHZ-II, HHZ-III)May 17, 2022
K202319Insulin Pen Needle (Ordinary Type), Insulin Pen Needle (Safety Type)November 12, 2021