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Shenzhen Ulike Smart Electronics Co., Ltd.

22 FDA records filed under this company name, from 2022 to 2026, in hair removal (OHT, 18), light for wrinkles (OHS, 3), microcurrent and ems (NFO, 1).

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, 18)

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)

510(k) number
K261325
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK)

510(k) number
K260742
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the long-lasting reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

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;UI20 BK, UI20 BL, UI20 BR, UI20 BS, UI20 DB, UI20 GP, UI20 GR, UI20 MP, UI20 PN, UI20 PW, UI20 RE, UI20 WH; UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB,UI06 PR, UI06 OG,UI06RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG; UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU; UI04 MK, UI04 BN, UI04 BU, UI04 CB, UI04 GY, UI04 LG, UI04 DG, UI04 PL,

510(k) number
K252804
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)

510(k) number
K251984
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK, UI20 DB, UI20 RE, UI20 PW, UI20 GP, UI20 GR, UI20 BK)

510(k) number
K250942
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK;UI04S PP, UI04S BU, UI04S WH, UI04S PN)

510(k) number
K250938
Applicant
Shenzhen Ulike Smart Electronics 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 4.

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH)

510(k) number
K250194
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

Copied from the text of FDA's 510(k) document (PDF, page 6), with line breaks removed.

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP)

510(k) number
K241998
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)

510(k) number
K242039
Applicant
Shenzhen Ulike Smart Electronics 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 4.

510(k) cleared

Ice Cooling IPL Hair Removal Device (Y6S GR, Y6S GA,Y6S GT, Y6S JU, Y6S JM, Y6S MU, Y6S OG, Y6S CH,Y6S PN,Y6S NK, Y6S PG, Y6S TG, Y6S OE)

510(k) number
K241205
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI07 BR, UI07 DB, UI07 BL, UI07 GP, UI07 PN, UI07 RE, UI07 WH, UI07 PW, UI20 BR, UI20 DB, UI20 BL, UI20GP, UI20 PN, UI20 RE, UI20 WH, UI20 PW)

510(k) number
K240649
Applicant
Shenzhen Ulike Smart Electronics 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 4.

510(k) cleared

Ice Cooling IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG,UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG, UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)

510(k) number
K240652
Applicant
Shenzhen Ulike Smart Electronics 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

“Ice Cooling IPL Hair Removal Device with sapphire treatment window is indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

IPL Hair Removal Device (UI06PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD, UI08 BR, UI08 DB, UI08 BL, UI08 GP, UI08 PN, UI08 RE, UI08 WH, UI08 PW, UI07 BR, UI07 DB, UI07 BL, UI07 GP, UI07 PN, UI07 RE, UI07 WH, UI07 PW, UI20 BR, UI20 DB, UI20 BL, UI20 GP, UI20 PN, UI20 RE, UI20 WH, UI20 PW)

510(k) number
K233887
Applicant
Shenzhen Ulike Smart Electronics 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 indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY,UI06 IG,)

510(k) number
K233664
Applicant
Shenzhen Ulike Smart Electronics 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 4.

510(k) cleared

IPL Hair Removal Device (UI04 MK,UI04 BN,UI04 BU,UI04 CB,UI04 GY,UI04 LG,UI04 DG,UI04 PL,UI04 PN,UI04 SD,UI04 SG,UI04 MG)

510(k) number
K233679
Applicant
Shenzhen Ulike Smart Electronics 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 indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime.”

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

510(k) cleared

IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG

510(k) number
K230122
Applicant
Shenzhen Ulike Smart Electronics 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 indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

IPL Hair Removal Device, Model(s): UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD

510(k) number
K223618
Applicant
Shenzhen Ulike Smart Electronics 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 indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

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

510(k) cleared

IPL Hair Removal Device, Model(s): UI04A, UI04B, UI04C

510(k) number
K221002
Applicant
Shenzhen Ulike Smart Electronics 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 indicated for the removal of unwanted hair. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months after the completion of a treatment regime.”

Copied from the text of FDA's 510(k) document (PDF, page 5), with line breaks removed.

LED and light devices for wrinkles (OHS, 3)

510(k) cleared

Ulike Reglow Light Therapy Device (UM10)

510(k) number
K260511
Applicant
Shenzhen Ulike Smart Electronics 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

“Ulike Reglow Light Therapy Device is an Over the Counter device that is intended for the use in the treatment of full face wrinkles and treatment of mild to moderate inflammatory acne.”

Copied from the text of FDA's 510(k) document (PDF, page 6), with line breaks removed.

510(k) cleared

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)

510(k) number
K251825
Applicant
Shenzhen Ulike Smart Electronics 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

“Jmoon FlexGlow Light Therapy Device is an over the counter device that is intended: - the Red light and Infrared light is indicated for use in the treatment of full face wrinkles, - the Blue light and Red light indicated for the treatment of mild to moderate inflammatory acne.”

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

510(k) cleared

Ulike Reglow Light Therapy Device (UM10)

510(k) number
K243492
Applicant
Shenzhen Ulike Smart Electronics 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

“Ulike Reglow Light Therapy Device is an over the counter device that is intended for use in the treatment of full face wrinkles and treatment of mild to moderate inflammatory acne.”

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

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

510(k) cleared

JMOON NouvelleSkin Facial Toning Device (M30U PR, M30U MW, M30U SG, M30U SK, M30U MP)

510(k) number
K243393
Applicant
Shenzhen Ulike Smart Electronics 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

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.