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Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

4 FDA records filed under this company name, from 2021 to 2024, in hair removal (OHT, 4).

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, 4)

510(k) clearedJun 18, 2024

IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)

510(k) number: K240583
Applicant: Shenzhen Beauty Every Moment Intelligent Electric 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 1, 2024

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) clearedMay 12, 2022

IPL Home Use Hair Removal Device

510(k) number: K221001
Applicant: Shenzhen Beauty Every Moment Intelligent Electric 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 4, 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)

510(k) clearedDec 20, 2021

IPL Home Use Hair Removal Device

510(k) number: K211185
Applicant: Shenzhen Beauty Every Moment Intelligent Electric 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, 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 5), with line breaks removed.

FDA database record FDA document (PDF)

510(k) clearedSep 20, 2021

IPL Home Use Hair Removal Device

510(k) number: K211922
Applicant: Shenzhen Beauty Every Moment Intelligent Electric 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: Jun 21, 2021

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 5), with line breaks removed.

FDA database record FDA document (PDF)