Data / Medical devices / China / Beatles Medical Supplies (xiantao) Co., Ltd
Beatles Medical Supplies (xiantao) Co., Ltd: FDA-registered device maker in Xiantao Hubei, China, 1 510(k) clearance
Beatles Medical Supplies (xiantao) Co., Ltd is registered with the FDA (registration 3021374000) in Xiantao Hubei, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021374000
- Address
- Louhe Industrial Park, Louhe Town, Xiantao Hubei, China, 433006
- Owner or operator
- Beatles medical supplies (Xiantao) Co., Ltd (10083670)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- December 13, 2021
- Registered through
- 2026
- Brand names listed
- Disposable Surgical Face Mask (3P00B, C2900), Face Masks (Cranberry Carbon 4-PLY), Face Masks (Cranberry S3+ Black / Blue / White), Face Masks (beesure 2100 Blue/White/Yellow), Fish shaped mask (Cranberry Fish shaped mask Blue/Black/Grey/Green)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| January 12, 2026 | K252830 | Disposable Surgical Face Mask (3P00B, C2900) | FXX | Substantially Equivalent | Beatles Medical Supplies (Xiantao) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 12, 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.