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IPL Hair Removal Device - UI06 RD
FDA 510(k)Class II (US FDA 510(k))
510(k) K233887
Identifiers
- 510(k) Number
- K233887 FDA 510(k)
- FDA Product Code
- OHT FDA 510(k)
- Models / Variants
- UI06PN FDA 510(k)UI06 PL FDA 510(k)UI06 JL FDA 510(k)UI06 BR FDA 510(k)UI06 DB FDA 510(k)UI06 PR FDA 510(k)UI06 OG FDA 510(k)UI06 RD FDA 510(k)UI08 BR FDA 510(k)UI08 DB FDA 510(k)UI08 BL FDA 510(k)UI08 GP FDA 510(k)UI08 PN FDA 510(k)UI08 RE FDA 510(k)UI08 WH FDA 510(k)UI08 PW FDA 510(k)UI07 BR FDA 510(k)UI07 DB FDA 510(k)UI07 BL FDA 510(k)UI07 GP FDA 510(k)UI07 PN FDA 510(k)UI07 RE FDA 510(k)UI07 WH FDA 510(k)UI07 PW FDA 510(k)UI20 BR FDA 510(k)UI20 DB FDA 510(k)UI20 BL FDA 510(k)UI20 GP FDA 510(k)UI20 PN FDA 510(k)UI20 RE FDA 510(k)UI20 WH FDA 510(k)UI20 PW 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 - UI06 RD by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 32 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 | K233887 | Class II | Active |
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Manufacturer
- Manufacturer
- Shenzhen Ulike Smart Electronics Co., Ltd.
Sources (1)
- FDA 510(k) K233887 24 fields · synced Jun 18, 2026