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Shenzhen Qianyu Technology Co., Ltd.

7 FDA records filed under this company name, from 2022 to 2026, in light for wrinkles (OHS, 3), microcurrent and ems (NFO, 1), 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.

LED and light devices for wrinkles (OHS, 3)

510(k) cleared

LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED Light Therapy Mask (JML5, JML5+JML7); LED Light Therapy Mask (JML6, JML6+JML8); LED Light Therapy Mask ( JML9, JML9+JML10)

510(k) number
K261851
Applicant
Shenzhen Qianyu Technology Co., Ltd.
Product code
OHS: Light Based Over The Counter Wrinkle Reduction
Regulation
21 CFR 878.4810, Class II
FDA decision
Substantially Equivalent (SESE)
Received

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 recordFDA document (PDF)

510(k) cleared

Wrinkle Treatment Device (JM1, JM2B)

510(k) number
K244020
Applicant
Shenzhen Qianyu Technology Co., Ltd.
Product code
OHS: Light Based Over The Counter Wrinkle Reduction
Regulation
21 CFR 878.4810, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use, as filed

“The Wrinkle Treatment Device is an Over-the-Counter (OTC) light based device intended for the use in treating full-face wrinkles.”

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

FDA database recordFDA document (PDF)

510(k) cleared

Wrinkle Treatment Device (JM2)

510(k) number
K240360
Applicant
Shenzhen Qianyu Technology Co., Ltd.
Product code
OHS: Light Based Over The Counter Wrinkle Reduction
Regulation
21 CFR 878.4810, Class II
FDA decision
Substantially Equivalent (SESE)
Received

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 4.

FDA database recordFDA document (PDF)

Electrical stimulation for aesthetic use (microcurrent and EMS) (NFO, 1)

510(k) cleared

JOVS Electric Stimulation Beauty Device (JE2)

510(k) number
K250227
Applicant
Shenzhen Qianyu Technology Co., Ltd.
Product code
NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use, as filed

“JOVS Electric Stimulation Beauty Device is indicated for over-the-counter aesthetic use including facial and neck stimulation.”

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

FDA database recordFDA document (PDF)

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

510(k) cleared

IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9

510(k) number
K231800
Applicant
Shenzhen Qianyu 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

Indications for use, as filed

“IPL 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 3), with line breaks removed.

FDA database recordFDA document (PDF)

510(k) cleared

Hand-held IPL device (JOVS Hair Removal Device)

510(k) number
K220645
Applicant
Shenzhen Qianyu 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

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 recordFDA document (PDF)

510(k) cleared

Hand-held IPL device(JOVS Graphene Hair Removal Device)

510(k) number
K214113
Applicant
Shenzhen Qianyu 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

Indications for use, as filed

“The Hand-held IPL device (JOVS Graphene 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 recordFDA document (PDF)