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IPL Hair Removal Device - UI04 SD

FDA 510(k)

Class II (US FDA 510(k))

510(k) K233679

by Shenzhen Ulike Smart Electronics Co., Ltd.

Identifiers

510(k) Number
K233679 FDA 510(k)
FDA Product Code
OHT FDA 510(k)
Models / Variants
UI04 MK FDA 510(k)
UI04 BN FDA 510(k)
UI04 BU FDA 510(k)
UI04 CB FDA 510(k)
UI04 GY FDA 510(k)
UI04 LG FDA 510(k)
UI04 DG FDA 510(k)
UI04 PL FDA 510(k)
UI04 PN FDA 510(k)
UI04 SD FDA 510(k)
UI04 SG FDA 510(k)
UI04 MG FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4810 FDA 510(k)
Regulation Number
878.4810 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

IPL Hair Removal Device - UI04 SD by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 12 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Shenzhen Ulike Smart Electronics Co., Ltd.

Sources (1)

  • FDA 510(k) K233679 24 fields · synced Jun 19, 2026