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Shenzhen Qiaochengli Technology Co., Ltd.

3 FDA records filed under this company name, from 2021 to 2025, 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) clearedOct 14, 2025

IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S)

510(k) number: K252234
Applicant: Shenzhen Qiaochengli 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: Jul 17, 2025

Indications for use, as filed

“IPL Home Use Hair Removal Device 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) clearedJun 2, 2022

IPL Hair Removal

510(k) number: K220927
Applicant: Shenzhen Qiaochengli 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: Mar 31, 2022

Indications for use

Not quoted here. We couldn't find a clean, complete statement in FDA's PDF, so we don't quote one. Read FDA's PDF.

FDA database record FDA document (PDF)

510(k) clearedSep 1, 2021

IPL Hair Removal

510(k) number: K211174
Applicant: Shenzhen Qiaochengli 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 20, 2021

Indications for use

Not quoted here. The statement contains words we couldn't confirm (a typo, run-together words or a reading error), and we don't correct FDA's text. Read FDA's PDF, page 5.

FDA database record FDA document (PDF)