Hironic Co., Ltd.

Hironic Co., Ltd. holds 9 FDA 510(k) medical device clearances, first cleared 2018, most recent 2026.

Top product codes for Hironic Co., Ltd.

Recent clearances by Hironic Co., Ltd.

K260387 — SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)Code NFO·2026-08-31
K260397 — SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002)Code GEI·2026-04-06
K251334 — NEW DOUBLO 2.0Code GEI·2025-09-29
K241099 — Plasonic (Plasonic)Code GEI·2024-11-08
K233123 — SILKROCode GEI·2024-06-24
K210084 — SILKROCode GEI·2022-06-03
K201773 — PICOHICode GEX·2021-10-19
K192970 — SLIMUSCode PKT·2020-12-01
K173676 — A-FITCode GEX·2018-09-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.