Data / Medical devices / China / Hubei Yjt Intelligent Technology Group Co., Ltd.
Hubei Yjt Intelligent Technology Group Co., Ltd.: FDA-registered device maker in Wuhan Hubei, China, 4 510(k) clearances
Hubei Yjt Intelligent Technology Group Co., Ltd. is registered with the FDA (registration 3011258423) in Wuhan Hubei, China. It lists 12 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 16, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3011258423
- Address
- Room 1-4, 8F, Block 7, Guannan Fuxing Pharmacel Park No.58, Optics Valley Avenue, East Lake High-tech Development Zone, Wuhan Hubei, China, 430074
- Owner or operator
- HUBEI YJT INTELLIGENT TECHNOLOGY GROUP CO., LTD. (formerly k (10049094)
- Roles
- Complaint file establishment, Contract manufacturer, Manufacturer
- First device listed
- April 13, 2015
- Registered through
- 2026
- Brand names listed
- BIOLUX Light Therapy Wand (Model: LP-BLUX), BIOLUX Light Therapy Wand Model: LP-BLUX, BIOREJUVENATE Red Light Nasal Therapy Model: LP-BRJVNT-BLK, BS001 Arm Sling, BeLight Handheld Device Model: D810, Biorecover Pro Light Therapy Knee Massager With Heat Model:LP-BRCVP-SLV, Blue Light Beauty Device Models :SZD-01,T100,YS-012,T115,MRD-201,DQ-LLD007,D360, Blue Light Beauty Device model:MHD003,MHD144 ,MHD005,MHD006,MHD007 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Attachment, Precision, All | EGG | 1 | Manufacturer | accessdata.fda.gov |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Manufacturer | accessdata.fda.gov |
| Joint, Shoulder, External Limb Component | IQQ | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | CCQ | 1 | Manufacturer | accessdata.fda.gov |
| Positioner, Tooth, Preformed | KMY | 1 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy | NHN | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Nebulizer, Electrically Powered | JPW | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Tonsil Suction | KCB | 1 | Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 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 |
|---|---|---|---|---|---|---|
| June 16, 2026 | K253231 | Laser Hair Growth System (Laser Cap 128, Laser Helmet 272, Laser Helmet 352, Laser Helmet 552, Laser Helmet 500) | OAP | Substantially Equivalent | Hubei Yjt Technology Co.,Ltd | accessdata.fda.gov |
| October 24, 2023 | K232356 | Laser Cap, Model: Hat-01 | OAP | Substantially Equivalent | Hubei Yjt Technology Co.,Ltd | accessdata.fda.gov |
| May 23, 2023 | K230134 | Laser Therapy Hair Growth Comb, Model: Lasercomb-001 & Lasercomb-002 | OAP | Substantially Equivalent | Hubei Yjt Technology Co.,Ltd | accessdata.fda.gov |
| February 6, 2002 | K010175 | MICROLIGHT 830 LASER SYSTEM | NHN | Substantially Equivalent | Microlight Corporation of America | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- All makers of Joint, Shoulder, External Limb Component
- All makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
- All makers of Laser, Comb, Hair
- All makers of Attachment, Precision, All
Updated June 16, 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.