Irestore

The iRestore Professional 282 is indicated to promote hair growth in males who have Norwood-Hamilton Classifications of IIa-V and in females with androgenetic alopecia who have Ludwig-Savin…

Registry build 21.09.26

The iRestore Professional 282 is indicated to promote hair growth in males who have Norwood-Hamilton Classifications of IIa-V and in females with androgenetic alopecia who have Ludwig-Savin Classifications I-II, and in both with Fitzpatrick Skin Phototypes I-IV.

30manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (18), Zhejiang (2), Jiangsu (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OAP
Manufacturer City Province Registered as Device types
Shenzhen Kaiyan Medical Equipment Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
Shenzhen Jie Zhong Lian Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
Zhejiang Runqiang Medical Instruments Co., Ltd. Jiaxing Zhejiang Contract manufacturer 9
Shenzhen Allbeauty Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 17
Hebei Tuosite Technology Co., Ltd. Shijiazhuang Hebei Manufacturer 14
Guangdong Fuqiang Beauty Equipment Co., Limited Qingyuan Guangdong Manufacturer 13
Dongguan Tutamen Metalwork Co., Ltd. Dongguan Guangdong Contract manufacturer 12
Hubei YJT Intelligent Technology Group Co., Ltd. Wuhan Hubei Contract manufacturer 12
Shenzhen Willcareyou Technology Co., Ltd. Shenzhen Guangdong Remanufacturer 10
VIS (Shanghai) Technology Co., Ltd. Jinshan District Shanghai Manufacturer 10
Zdeer Technology (Henan) Co., Ltd. Xuchang Henan Remanufacturer 9

Showing 12 of 30. All 30 manufacturers in China registered for Laser, Comb, Hair

Record

Regulatory record for iRestore
Listed by Freedom Laser Therapy, Inc., United States
FDA product code OAP
Device type Laser, Comb, Hair
Device class Class 2
Regulation 21 CFR 890.5500
Record published 2019-07-09
Record revised 2020-07-07 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Over the counter Yes
Label carries manufacturing date, serial number
Packaging Pack of 4

Catalogue Numbers

Catalogue numbers for iRestore
Catalogue number Size Status
ID-505 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Capillus Capillus, LLC 29
HairMax Lexington Medical, Inc. 16
Xtrallux™ Xtrallux, LLC 9
CurrentBody Skin™ Shenzhen Kaiyan Medical Equipment Co., Ltd. 6
Kernel Xuzhou Kernel Medical Equipment Co Ltd 5
Diode Laser Cap Cosmo FAR East Technology Limited 4
RedRestore 10589578 Canada Inc. 4
Newhair Laser Hair Growth CAP Shang FAR Biotechnology Co. 4
iRestore Remax Medi-Tech(Shenzhen) Corporation 3
Hairclub RX™ Xtrallux, LLC 3
Hair Growth Device Dongguan Boyuan Intelligent Technology Co., Ltd. 2
Medi Tresse LaserCap HD LaserCap Company 2

Showing 12 of 66. All products under Laser, Comb, Hair

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K222081 2022-10-13
K213094 2021-12-22
K183417 2019-05-17
K151662 2016-01-06

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer