Sunny Plus (Sunny)— 510(k) K251649

Substantially Equivalent

ShenB Co., Ltd.

FDA 510(k) clearance K251649 for Sunny Plus (Sunny), Substantially Equivalent on 2025-09-18. Applicant: ShenB Co., Ltd.. Device class: 2.

Clearance details

Applicant: ShenB Co., Ltd.
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-05-29
Decision date: 2025-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seoul, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code NFO

K262861 — PureLift Pro Max2026-09-11
K260387 — SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)2026-08-31
K253932 — FACEGYM Pro Device (HD-109)2026-07-23
K260179 — VITA Multi-Function Head Brush (TB-2343F, TB-2442F)2026-06-03
K260895 — Ulike Clear Zero (YC10 BU)2026-05-28

More clearances from ShenB Co., Ltd.

K253926 — Diacore2026-04-10
K242241 — Sunny2025-03-19
K241535 — Vybe RF II2024-09-25
K232223 — PlaDuo System2023-10-24
K230968 — VYBE RF Electrosurgical System2023-07-06

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