Data / Medical devices / China / Zdeer Technology (henan) Co., Ltd
Zdeer Technology (henan) Co., Ltd: FDA-registered device maker in Xuchang City Henan, China, 2 510(k) clearances
Zdeer Technology (henan) Co., Ltd is registered with the FDA (registration 3033905868) in Xuchang City Henan, China. It lists 9 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 16, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033905868
- Address
- East of Wei Wu Road and south of Qin Gong East Road, Toubao Village Committee, Laotown Town, Changge, Xuchang City Henan, China, 461500
- Owner or operator
- Zdeer Technology (Henan) Co., Ltd (10091906)
- Roles
- Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler
- First device listed
- November 14, 2024
- Registered through
- 2026
- Brand names listed
- ARTISTIC TOOTHBRUSH; ZD-D401-Matte Finish Version, Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155), Bone Conduction Hearing Aid (G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155), Bone Conduction Hearing Aid (G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160), Bone Conduction Hearing Aid (G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158), DIGITAL HEARING AIDS(BG11151, BG11152, BG11153, BG11154, BG11155, BG11156, BG11157, BG11158, BG11159, BG11160), DIGITAL HEARING AIDS(BG11161, BG11162, BG11163, BG11164, BG11165, BG11166, BG11167, BG11168, BG11169, BG11170), DIGITAL HEARING AIDS(BG11171, BG11172, BG11173, BG11174, BG11175, BG11176, BG11177, BG11178, BG11179, BG11180) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Clinical Electronic Thermometer | SDV | 2 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | QUG | 2 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Over The Counter | QUF | 1 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Hearing Aid, Bone Conduction | LXB | 2 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | 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 | K260899 | Laser Hair Growth Device (F21151, F21152, F21153, F21154, F21155, F21156, F21157, F21158, F21159) | OAP | Substantially Equivalent | Zdeer Technology (Henan) Co., Ltd. | accessdata.fda.gov |
| June 15, 2026 | K260452 | Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155, G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155, G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160, G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158) | LXB | Substantially Equivalent | Zdeer Technology (Henan) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Laser, Comb, Hair
- All makers of Toothbrush, Manual
- All makers of Clinical Electronic Thermometer
- All makers of Hearing Aid, Air-Conduction, Over The Counter
- All makers of Hearing Aid, Bone Conduction
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
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.