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Shenzhen Semlamp Intelligent Technology Co., Ltd.

3 FDA records filed under this company name, from 2022 to 2026, in hair removal (OHT, 3).

The applicant is the company that filed with FDA. It can be the brand you know or a manufacturer that makes devices sold under other brand names; the device name as filed often shows which. We don't merge different company names, so check the A–Z list for related entries.

Laser and IPL hair removal (mostly over-the-counter; 1 record says prescription use) (OHT, 3)

510(k) clearedApr 21, 2026

IPL Hair Removal (SL-B301, SL-B300, SL-B330, SL-B330-1, SL-B287-1, SL-B371, SL-B371-2, SL-B371-1, SL-B352, SL-B352-1, SL-B352-2, SL-B330-F)

510(k) number: K260518
Applicant: Shenzhen Semlamp Intelligent Technology Co., Ltd.
Product code: OHT: Light Based Over-The-Counter Hair Removal
Regulation: 21 CFR 878.4810, Class II
FDA decision: Substantially Equivalent (SESE)
Received: Feb 17, 2026

Indications for use, as filed

“The IPL Hair Removal is an over-the-counter device intended for removal of unwanted body and/or facial hair.”

Copied from the text of FDA's 510(k) document (PDF, page 4), with line breaks removed.

FDA database record FDA document (PDF)

510(k) clearedMay 31, 2024

IPL Hair Removal (SL-B287, SL-B329, SL-B301-1, SL-B328)

510(k) number: K240969
Applicant: Shenzhen Semlamp Intelligent Technology Co., Ltd.
Product code: OHT: Light Based Over-The-Counter Hair Removal
Regulation: 21 CFR 878.4810, Class II
FDA decision: Substantially Equivalent (SESE)
Received: Apr 9, 2024

Indications for use, as filed

“The IPL Hair Removal is an over the-counter device intended for removal of unwanted body and/or facial hair.”

Copied from the text of FDA's 510(k) document (PDF, page 3), with line breaks removed.

FDA database record FDA document (PDF)

510(k) clearedJul 7, 2022

IPL Hair Removal (Model: SL-B080, SL-B126, SL-B136)

510(k) number: K221246
Applicant: Shenzhen Semlamp Intelligent Technology Co., Ltd.
Product code: OHT: Light Based Over-The-Counter Hair Removal
Regulation: 21 CFR 878.4810, Class II
FDA decision: Substantially Equivalent (SESE)
Received: May 2, 2022

Indications for use

Not quoted here. The page with this statement is a scanned image whose text was machine-read, so we can't vouch for it word for word. Read FDA's PDF, page 3.

FDA database record FDA document (PDF)