Data / Medical devices / China / Huizhou Jinghao Medical Technology Co., Ltd
Huizhou Jinghao Medical Technology Co., Ltd: FDA-registered device maker in Huizhou Guangdong, China, 1 510(k) clearance
Huizhou Jinghao Medical Technology Co., Ltd is registered with the FDA (registration 3011586575) in Huizhou Guangdong, China. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 25, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3011586575
- Address
- No. 207, South SiHuan Rd, ZhongKai Hi-tech District, Huizhou Guangdong, China, 516000
- Owner or operator
- Huizhou Jinghao Medical Technology Co., Ltd (10048535)
- Roles
- Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- January 23, 2015
- Registered through
- 2026
- Brand names listed
- Hearing aid,amplifiers with models JH-A17BT,JH-A32BT,JH-A39HT,JH-A61AT, JH-A62AT,JH-D26AT,JH-D35CT,JH-D59CT,JH-D12AT, Hearing aid,amplifiers with models JH-AW2BT,JH-TW4AT,JH-DW1AT,JH-DW2AT,JH-DW3FT,JH-DW4AT,JH-D13B,JH-A36D, Hearing aid,amplifiers with models JH-DW1A, JH-DW3A, JH-125,JH-115,JH-338, JH-A170, JH-A19A,BRH -007,BRH -124, JH-D36AT,JH-A17CT,JH-DW2ET,JH-A49A,JH-A490,CE-A18A,CE-A80B,JH-DW4E,JH-A260,JH-A26A,CE-A90A,JH-D260,JH-A420,JH-A26D, JH-D58,JH-DW3F,JH-DW5A and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | QUG | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction With Wireless Technology, Prescription | OSM | 2 | Complaint file establishment, Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Over The Counter | QUF | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Prescription | ESD | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Self-Fitting Air-Conduction Hearing Aid, Over The Counter | QUH | 2 | 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 |
|---|---|---|---|---|---|---|
| September 25, 2023 | K221052 | Self-Fitting hearing aids | QUH | Substantially Equivalent | Huizhou Jinghao Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Hearing Aid, Air-Conduction, Prescription
- All makers of Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter
- All makers of Hearing Aid, Air-Conduction With Wireless Technology, Prescription
- All makers of Self-Fitting Air-Conduction Hearing Aid, Over The Counter
- All makers of Hearing Aid, Air-Conduction, Over The Counter
Updated September 25, 2023. 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.