Data / Medical devices / China / Huizhou Anboson Technology Co., Ltd.
Huizhou Anboson Technology Co., Ltd.: FDA-registered device maker in huizhou Guangdong, China, 1 510(k) clearance
Huizhou Anboson Technology Co., Ltd. is registered with the FDA (registration 3017929385) in huizhou Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017929385
- Address
- 2 / F, factory building No.7, Hechang East 4th Road, Zhongkai hi tech Zone, Huizhou City, huizhou Guangdong, China, 516001
- Owner or operator
- Huizhou ANBOSON Technology Co., Ltd. (10079802)
- Roles
- Manufacturer
- First device listed
- January 14, 2022
- Registered through
- 2026
- Brand names listed
- Disposable Examination Gloves, Latex patient examination glove, Patient examination glove, Polymer patient examination glove
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Latex Patient Examination Glove | LYY | 1 | Manufacturer | accessdata.fda.gov |
| Patient Examination Glove | FMC | 1 | Manufacturer | accessdata.fda.gov |
| Polymer Patient Examination Glove | LZA | 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 |
|---|---|---|---|---|---|---|
| May 31, 2023 | K230542 | Disposable Nitrile Gloves (ABC-DG01) | LZA | Substantially Equivalent | Huizhou Anboson Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Polymer Patient Examination Glove
- All makers of Patient Examination Glove
- All makers of Latex Patient Examination Glove
Updated May 31, 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.