Data / Medical devices / China / Guangzhou Ahead Intelligent Technology Co., Ltd.
Guangzhou Ahead Intelligent Technology Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 1 510(k) clearance
Guangzhou Ahead Intelligent Technology Co., Ltd. is registered with the FDA (registration 3019864920) in Guangzhou Guangdong, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019864920
- Address
- Room 304, Building 4, No. 9 Shinan Second Road, Huijiang Village, Dashi Street, Panyu District, Guangzhou Guangdong, China, 511400
- Owner or operator
- Guangzhou Ahead Intelligent Technology Co., Ltd. (10089647)
- Roles
- Manufacturer
- First device listed
- December 26, 2023
- Registered through
- 2026
- Brand names listed
- A10N,A6S11E,H3PIN,A9N,G1,G2,G3,G4,G5,G6,G7,G8,G9,G10,A6S,M8S,M7S,M6S,M9S,140A,64A,HN20,HN30,H24, BN120,BIO4,N2,M5,M7,M8,M9,A1,A6,A7,A8S,A9,A10,A11,A12,A13,A14,A15,A16,A17,A18,A19,A20,H2,H3,H5,H6,H7,H8,H9, Beauty Massager: X1, X2, X3, X4, X5, X6, X7, X8, X9, X1S, X2S, X3S, X4S, X5S, X6S, X7S, X8S, X9S, Derma Infusion Pen: DMJW01-DMJW13, DMJL01-DMJL13, DMJC01-DMJC09, DMJD05-DMJD13, DPM811-DPM819, Headache Relief Cap: H10,H20,H30,H40,H50,H60,H70,H80,H90,H10S,H20S,H30S,H40S,H50S,H60S,H70S,H80S,H90S, Hydrating Eye Compress: E100, E200, E300, E400, E500, E600, E700, E800, E900, E100S, E200S, E300S, E400S,E500S, E600S,, Hydrating Eye Compress: E700S, E800S, E900S, Ice Roller: IR1001-IR1012, S10, S20, S30, S40, S50, S60, S70, S80, S90, S100 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 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 6, 2025 | K251042 | Light Therapy System (M500, L6) | OHS | Substantially Equivalent | Guangzhou Ahead Intelligent Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Pack, Hot Or Cold, Reusable
- All makers of Massager, Therapeutic, Manual
- 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 Lamp, Infrared, Therapeutic Heating
- All makers of Needle, Acupuncture, Single Use
Updated June 6, 2025. 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.