JMOON NouvelleSkin Facial Toning Device (M30U PR +4 more)

FDA 510(k)

Class II (US FDA 510(k))

510(k) K243393

by Shenzhen Ulike Smart Electronics Co., Ltd.

Identifiers

510(k) Number: K243393 FDA 510(k)
FDA Product Code: NFO FDA 510(k)
Models / Variants: M30U PR FDA 510(k)
M30U MW FDA 510(k)
M30U SG FDA 510(k)
M30U SK FDA 510(k)
M30U MP FDA 510(k)

Classification

Device Class: Class II FDA 510(k)
Legislation / Framework: 21 CFR Part 882.5890 FDA 510(k)
Regulation Number: 882.5890 FDA 510(k)
Advisory Committee: Neurology FDA 510(k)
FDA Decision: SESE Substantially Equivalent FDA 510(k)

JMOON NouvelleSkin Facial Toning Device (M30U PR +4 more) by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 5 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Source	Region	Type	Cert / Approval No.	Class	Status
FDA 510(k)	United States	FDA_510K	K243393	Class II	Active

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Manufacturer

Manufacturer: Shenzhen Ulike Smart Electronics Co., Ltd.

Sources (1)

FDA 510(k) K243393 24 fields · synced Jun 19, 2026