Hironic Co., Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Hironic Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Latest FDA clearance: Apr 2026. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hironic Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by E & M as regulatory consultant.
8 devices
Cleared
Apr 06, 2026
SYNERJET PRO (SP-1002)
General & Plastic Surgery
59d
Cleared
Sep 29, 2025
NEW DOUBLO 2.0
General & Plastic Surgery
152d
Cleared
Nov 08, 2024
Plasonic (Plasonic)
General & Plastic Surgery
200d
Cleared
Jun 24, 2024
SILKRO
General & Plastic Surgery
271d
Cleared
Jun 03, 2022
SILKRO
General & Plastic Surgery
507d
Cleared
Oct 19, 2021
PICOHI
General & Plastic Surgery
477d
Cleared
Dec 01, 2020
SLIMUS
General & Plastic Surgery
405d
Cleared
Sep 14, 2018
A-FIT
General & Plastic Surgery
288d