Data / Medical devices / China / Allwin First Aid Supplies Taizhou Co., Ltd
Allwin First Aid Supplies Taizhou Co., Ltd: FDA-registered device maker in Taizhou Jiangsu, China, 1 510(k) clearance
Allwin First Aid Supplies Taizhou Co., Ltd is registered with the FDA (registration 3045078803) in Taizhou Jiangsu, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 21, 2018. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3045078803
- Address
- Room 101, Building 18, No. 99 Xianglong Road, Medical High-tech Zone, Taizhou Jiangsu, China, 225300
- Owner or operator
- ALLWIN FIRST AID SUPPLIES TAIZHOU CO., LTD (10095804)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- May 1, 2026
- Registered through
- 2026
- Brand names listed
- FIRST AID BAG, FIRST AID KIT, General First Aid Kit, Mini First Aid Kit, Trauma Kit, METAL FIRST AID BOX, PLASTIC FIRST AID BOX, VINYL PATIENT EXAMINATION GLOVES, DISPOSABLE VINYL GLOVES
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| First Aid Kit With Drug | LRR | N | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Vinyl Patient Examination Glove | LYZ | 1 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| September 21, 2018 | K182043 | Single-use medical poly (vinyl chloride) examination glove (Clear, Non-Colored) | LYZ | Substantially Equivalent | Hebei Titans Hongsen Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of First Aid Kit With Drug
- All makers of Vinyl Patient Examination Glove
- All makers of First Aid Kit Without Drug
Updated September 21, 2018. 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.