Data / Medical devices / China / Vis (shanghai) Technology Co., Ltd.
Vis (shanghai) Technology Co., Ltd.: FDA-registered device maker in Jinshan District Shanghai, China, 10 510(k) clearances
Vis (shanghai) Technology Co., Ltd. is registered with the FDA (registration 3016076077) in Jinshan District Shanghai, China. It lists 10 device types. The FDA files 10 510(k) clearances under its listings, the newest dated February 20, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016076077
- Address
- No. 58 Linsheng Road Tinglin Town, Jinshan District Shanghai, China, 201505
- Owner or operator
- VIS (Shanghai) Technology, Co. Ltd. (10066332)
- Roles
- Manufacturer
- First device listed
- April 1, 2020
- Registered through
- 2026
- Brand names listed
- BEAR, BEAR MINI, Bear 2, Bear 2 body, Bear 2 eyes & lips, Bear 2 go, ESPADA 2, ESPADA 2 PLUS and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Heat Source For Bleaching Teeth | EEG | 1 | Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction | PAY | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 20, 2026 | K253683 | FAQ (LED Panel); FAQ (Dual LED Panel) | OHS | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| December 11, 2024 | K242747 | FAQ (302) | OAP | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| August 20, 2024 | K241102 | Luna 4 plus | OHS | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| July 15, 2024 | K240616 | FAQ (102) | PAY | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| May 13, 2024 | K232242 | BEAR 2 Body | NFO | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| April 19, 2024 | K240378 | FAQ 201, FAQ 202 | OHS | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| September 25, 2023 | K231977 | PEACH 2, PEACH 2 Duo, PEACH 2 go | OHT | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| April 5, 2023 | K222012 | FAQ 101 | PAY | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| July 31, 2020 | K200803 | BEAR and BEAR mini | NFO | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
| November 30, 2016 | K162450 | ESPADA Acne-Clearing Blue Light Pen | OLP | Substantially Equivalent | Foreo, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Powered Laser Surgical Instrument
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Heat Source For Bleaching Teeth
Updated February 20, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.