← Product Code [OHT](/submissions/SU/subpart-e%E2%80%94surgical-devices/OHT) · K220669
# IPL HAIR REMOVAL HANDSET, Model: IPL-666 (K220669)
_Shenzhen Junbobeauty Technology Co., Ltd. · OHT · May 16, 2022 · General, Plastic Surgery · SESE_
**Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHT/K220669
## Device Facts
- **Applicant:** Shenzhen Junbobeauty Technology Co., Ltd.
- **Product Code:** [OHT](/submissions/SU/subpart-e%E2%80%94surgical-devices/OHT.md)
- **Decision Date:** May 16, 2022
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 878.4810
- **Device Class:** Class 2
- **Review Panel:** General, Plastic Surgery
- **Attributes:** Therapeutic
## Intended Use
IPL HAIR REMOVAL HANDSET is an over-the-counter device intended for removal of unwanted body and/or facial hair.
## Device Story
IPL HAIR REMOVAL HANDSET is a handheld, over-the-counter, light-based hair reduction device for home use. It utilizes a Xenon Quartz Lamp Tube to emit Intense Pulsed Light (IPL) to reduce hair growth without cutting or pulling. The device is powered by an external AC adapter and operated via a finger switch. It incorporates a skin sensor to ensure full contact with the treatment area before pulse emission is enabled. The device is intended for use on facial hair below the chin line, arms, legs, underarms, and bikini line. By delivering light energy to the skin, the device targets hair follicles to achieve hair reduction with minimal pain. Healthcare providers do not operate the device; it is intended for patient self-use. The device provides 5 intensity levels for user adjustment.
## Clinical Evidence
Bench testing only. No clinical data provided. Compliance verified via electrical safety (ANSI AAMI ES 60601-1, IEC 60601-1-2, IEC 60601-1-11, IEC 60601-2-83), photobiological safety (IEC 62471), and biocompatibility (ISO 10993-5, ISO 10993-10). Software verification and validation performed per FDA guidance.
## Technological Characteristics
Handheld IPL device; Xenon Quartz Lamp Tube; 470-1100nm wavelength; max 2.49 J/cm² energy density; 11.5-15ms pulse duration; 3cm² spot size. Powered by external 100-240V AC/12V 3A DC adapter. Materials: plastic/metal enclosure. Skin sensor for contact detection. Software-controlled pulse emission. Sterilization: not required.
## Regulatory Identification
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
## Predicate Devices
- IPL Salon Hair Reduction System, Model: F60001 ([K181568](/device/K181568.md))
## Reference Devices
- IPL Home Use Hair Removal Device, Model(s): D-1128, D-1103, D-1119, D-1129, D-1130 ([K192432](/device/K192432.md))
## Submission Summary (Full Text)
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May 16, 2022
Shenzhen Junbobeauty Technology Co., Ltd. % Tracy Che Registration Engineer Feiying Drug & Medical Consulting Technical Service Group Rm 2401 Zhenye International Business Center, No. 3101-90 Oianhai Road Shenzhen, Guangdong 518052 China
Re: K220669
Trade/Device Name: IPL HAIR REMOVAL HANDSET, Model: IPL-666 Regulation Number: 21 CFR 878.4810 Regulation Name: Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology Regulatory Class: Class II Product Code: OHT Dated: February 25, 2022 Received: March 7, 2022
Dear Tracy Che:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
Purva Pandya Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
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# Indications for Use
510(k) Number (if known) K220669
Device Name IPL HAIR REMOVAL HANDSET, Model: IPL-666
Indications for Use (Describe)
IPL HAIR REMOVAL HANDSET is an over-the-counter device intended for removal of unwanted body and/or facial hair.
| Type of Use (Select one or both, as applicable) |
|-------------------------------------------------|
|-------------------------------------------------|
Prescription Use (Part 21 CFR 801 Subpart D)
X Over-The-Counter Use (21 CFR 801 Subpart C)
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# 510 (k) Summary
This "510(k) Summary" of 510(k) safety and effectiveness information is submitted in accordance with requirements of Title 21, CFR Section 807.92.
### (1) Applicant information:
| 510(k) owner's name: | Shenzhen Junbobeauty Technology Co., Ltd. |
|---------------------------|--------------------------------------------------------------------------------|
| Address: | #522, Jinyuan Business Building A, Xixiang Blvd 300, Bao'an District, Shenzhen |
| Contact person: | Jian Zhan |
| Phone number: | +86 17665318870 |
| Fax number: | / |
| Email: | 779182481@qq.com |
| Date of summary prepared: | 2022-2-25 |
#### (2) Reason for the submission
New device, there were no prior submissions for the device.
#### (3) Proprietary name of the device
| Trade name/model: | IPL HAIR REMOVAL HANDSET, Model: IPL-666 |
|--------------------|-------------------------------------------|
| Common name: | Light Based Over-The-Counter Hair Removal |
| Regulation number: | 21 CFR 878.4810 |
| Product code: | OHT |
| Review panel: | General & Plastic Surgery |
| Regulation class: | Class II |
#### (4) Predicate and reference device
#### > Predicate device
| Sponsor | Medical Device Branch of Zhangzhou Easepal Industrial
Co.,Ltd. |
|-----------------------|-------------------------------------------------------------------|
| Device Name and Model | IPL Salon Hair Reduction System, Model: F60001 |
| 510(k) Number | K181568 |
| Product Code | OHT |
| Regulation Number | 21 CFR 878.4810 |
| Regulation Class | II |
| > Reference device | |
| Sponsor | Shenzhen Bosidin Technology Co. Ltd. |
| Device Name and Model | IPL Home Use Hair Removal Device |
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#### K220669
Shenzhen Junbobeauty Technology Co., Ltd. 510(k)s - Section 8. 510 (k) Summary
| Model(s): D-1128, D-1103, D-1119, D-1129, D-1130 | |
|--------------------------------------------------|-----------------|
| 510(k) Number | K192432 |
| Product Code | OHT |
| Regulation Number | 21 CFR 878.4810 |
| Regulation Class | II |
#### (5) Description/ Design of device:
The IPL HAIR REMOVAL HANDSET is a personal, light-based, hair reduction device intended to be sold over-the-counter directly to the end user. The device provides hair reduction using Intense Pulsed Light (IPL) technology. It works below the skin's surface and does not involve any cutting or pulling, reducing hair growth with minimal pain. The device is only powered by the external power adapter and its IPL emission activation is by finger switch. The device contains a Xenon Quartz Lamp Tube to emit light and a skin sensor to detect appropriate skin contact. If the device is not properly applied to the treatment area (in full contact with the skin), the device cannot trigger a pulse emitting.
The IPL HAIR REMOVAL HANDSET includes only one model IPL-666.
#### (6) Indications for use:
IPL HAIR REMOVAL HANDSET is an over-the-counter device intended for removal of unwanted body and/or facial hair.
#### (7) Materials
| Component
name | Material of Component | Body Contact Category | Contact Duration |
|----------------------------------------------------------------------|-----------------------|-------------------------------------------|--------------------|
| IPL HAIR
REMOVAL
HANDSET
(Enclosure
and flash
window) | Plastic, metal | Surface-contacting
device: Intact skin | Less than 24 hours |
We have tested the device for biocompatibility by a reliable third-party lab. For details, please refer to "Biocompatibility Discussion".
#### (8) Technological characteristics and substantial equivalence:
| Item | Subject device | Predicate device | Reference device | Remark |
|------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------|
| Trade name | IPL HAIR REMOVAL
HANDSET
Model: IPL-666 | IPL Salon Hair
Reduction System,
Model: F60001 | IPL Home Use Hair
Removal Device
Model(s): D-1128, | / |
| | | | | |
| 510 (k) number | Applying | K181568 | D-1103, D-1119,
D-1129, D-1130
K192432 | / |
| Manufacturer | Shenzhen Junbobeauty
Technology Co., Ltd. | Medical Device
Branch of Zhangzhou
Easepal Industrial
Co., Ltd. | Shenzhen Bosidin
Technology Co.,Ltd. | / |
| Regulation
number | 21CFR 878.4810 | 21CFR 878.4810 | 21CFR 878.4810 | Same |
| Product code | OHT | OHT | OHT | Same |
| Class | II | II | II | Same |
| Indications for
use/ Intended
use | IPL HAIR REMOVAL
HANDSET is an over-
the-counter device
intended for removal of
unwanted body and/or
facial hair. | The IPL Salon Hair
Reduction System
(Model: F60001) is an
over the Counter
device intended for
the removal of
unwanted body and/or
facial hair in adults. It
is also intended for
permanent reduction
in unwanted hair.
Permanent hair
reduction is defined as
the long-term stable
reduction in the
number of hairs
re-growing when
measured at 6. 9. and
12 months after the
completion of a
treatment regimen. | IPL Home Use Hair
Removal Device is an
over-the-counter device
intended for removal of
unwanted body and/or
facial hair. | Same |
| Prescription or
OTC | OTC | OTC | OTC | Same |
| Applicable skin | Fitzpatrick Skin
Phototypes I-V | Unknown | Fitzpatrick Skin
Phototypes I-V | Same |
| Treatment area | Used on facial hair
below the chin line,
arms, legs, underarms,
bikini line. | The device is
designed for use on
the legs, underarms,
bikini line, chest,
stomach, back, arms
and on the face below
the cheekbones | Removal of unwanted
body hair such as but
not limited to small
areas such as underarm
and facial hair below
the chin line and large
areas such as legs. | Similar |
| Device design | | | | |
| Power source | An external power supply | Supplied by external adapter | Supplied by external power adapter | Same |
| Power supply | 100~240V AC Input 12V3A DC Output | 100-240 V AC; 50/60 Hz | Input: 100-240V 50/60Hz 1.0-0.5A
Output: DC12V 3A | Different
Note 1 |
| Product compositions | IPL Hair Removal Handset and power adapter | Device includes a treatment window head, a facial adaptor and battery charger/ AC cord. | IPL host, lamp cartridge and power adapter | Similar |
| Structure design | Handheld | Handheld | Handheld | Same |
| Dimension | 124*83*48.5mm | 143 x69.5 x 43mm (H*W*D) | 218 x 144 x 60mm | Different
Note 2 |
| Weight | 186g | 650g | 355g | Different
Note 2 |
| Sterilization | Not required | Not required | Not required | Same |
| Output specification | | | | |
| Light source | Intense Pulsed Light | Intense Pulsed Light | Intense Pulsed Light | Same |
| Energy medium | Xenon Quartz Tube | Xenon Arc Flashlamp | Xenon lamp | Similar
Note 3 |
| Wavelength range (nm) | 470nm ~1100nm | 475nm~1200nm | Regular window: 510 ~ 1100nm
Filter window: 600 ~ 1100nm | Similar
Note 3 |
| Energy density (J/cm²) | Max 2.49J/cm² | Max 5J/cm² | 2.0~4.0J/cm²
(applicable for model D-1128, D-1119, D-1129, D-1130)
2.5~4.5J/cm²
(applicable for model D-1103) | Similar
Note 3 |
| Spot size (Size of treatment window) (cm²) | 3cm² | 1.72 cm² or 3.02 cm² | Regular window: 4.5cm², 2.0cm², 3.0cm²
Filter window: 2.5cm² | Same |
| Pulse duration | 11.5-15ms | 11-12ms | 7.5-14ms | Similar
Note 3 |
| Pulsing control | Finger switch | Finger switch | Finger switch | Same |
| Delivery device | Direct illumination to tissue | Direct illumination to tissue | Direct illumination to tissue | Same |
| Number of output channels | One channel | One channel | One channel | Same |
| Output | 5 levels | 5 levels | 5 levels | Same |
| intensity level | | | | |
| Skin sensor | Sensor fixed in handset
and can be moved to
treatment part | Sensor fixed in device
and can be moved to
treatment part | Sensor fixed in device
and can be moved to
treatment part | Same |
| Software/
Firmware/
Microprocessor
Control? | Yes | Yes | Yes | Same |
| Additional features | | | | |
| Skin-contacting
components | Plastic enclosure and
treatment window | IPL Lamp output
window | Plastic enclosure and
treatment window | Same |
| Materials of
skin-contacting
components | Plastic, metal | ABS | ABS, PC, Aluminium
alloy | Different
Note 4 |
| Biocompatibility | All user directly
contacting materials are
compliance with
ISO10993-5 and
ISO10993-10
requirements. | All user directly
contacting materials
are compliance with
ISO10993-5 and
ISO10993-10
requirements. | All user directly
contacting materials are
compliance with
ISO10993-5 and
ISO10993-10
requirements. | Same |
| Electrical
safety | IEC60601-1-2
IEC60601-1
IEC60601-1-11
IEC60601-2-83 | IEC 60601-1
IEC 60601-1-2
IEC60601-2-57 | IEC60601-1-2
IEC60601-1
IEC60601-1-11
IEC60601-2-57 | Similar |
| Photobiological
safety | IEC62471 | Unknown | IEC62471 | Same |
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## K220669
Shenzhen Junbobeauty Technology Co., Ltd.
510(k)s – Section 8. 510 (k) Summary
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Shenzhen Junbobeauty Technology Co., Ltd. 510(k)s - Section 8. 510 (k) Summary
#### Comparison in details:
#### Note 1:
The power adapter has been tested along with the subject device for electrical safety, so this difference will not raise any safety/ effectiveness problems.
#### Note 2:
Although the appearance, weight and dimensions are different between the subject and predicate device, these differences are insignificant and do not raise any safety/ effectiveness problems.
#### Note 3:
The energy medium are both Xenon lamp, although they are a little different, the output specification such as wavelength range, energy density, pulse duration are close to the predicate's device range, these parameters of the subject device can be basically covered by the predicate devices' range, they are very similar. So this difference will not raise any safety/ effectiveness problems.
#### Note 4:
Although the "Materials of skin-contacting components" of the subject device and predicate device are not exactly the same, the skin-contacting components of the subject device has been tested and satisfied the standard requirements of ISO 10993-1. So this difference will not raise any safety/ effectiveness problems.
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#### (9) Non-clinical studies and tests performed:
Non-clinical testings have been conducted to verify that the IPL HAIR REMOVAL HANDSET meets all design specifications which supports the conclusion that it's Substantially Equivalent (SE) to the predicate device. The testing results demonstrate that the subject device complies with the following standards:
- ANSI AAMI ES 60601-1, Medical electrical equipment Part 1: General requirements for A basic safety and essential performance
- A IEC 60601-1-2, Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests
- A IEC 60601-1-11, Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
- > IEC 60601-2-83, Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment
- > IEC 62471, Photobiological safety of lamps and lamp systems
The device has been tested for biocompatibility, it complies with the following standards.
- ISO 10993-5, Biological Evaluation of Medical Devices Part 5: Tests for InVitro A Cvtotoxicitv
- A ISO 10993-10, Biological Evaluation of Medical Devices - Part 10: Tests for Irritation and Skin Sensitization.
We have also conducted:
- Software verification and validation test according to the requirements of the FDA "Guidance A for Pre Market Submissions and for Software Contained in Medical Devices"
#### (10) Conclusion
Based on the above analysis and non-clinical tests performed, it can be concluded that the subject device IPL HAIR REMOVAL HANDSET is as safe, as effective, and performs as well as the legally marketed predicate device, IPL Salon Hair Reduction System.
---
**Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHT/K220669](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHT/K220669)
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