Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)— 510(k) K251825
Substantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.
FDA 510(k) clearance K251825 for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG), Substantially Equivalent on 2025-10-01. Applicant: Shenzhen Ulike Smart Electronics Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Ulike Smart Electronics Co., Ltd.
- Product code
- Code OHS
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code OHS
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- K260511 — Ulike Reglow Light Therapy Device (UM10)
- K252804 — Ice Cooling IPL Hair Removal Device (UI20S BK, UI20S BS, UI20S DB, UI20S GP, UI20S GR, UI20S MP, UI20S PW, UI20S RE, UI20S WH, UI20WG +4 more
- K251984 — Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)
Adverse events under product code OHS
product code OHS- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.