AOSHANG earloop
by Tianjin Aoshang Outdoor Equipment Co., Ltd. 6 variants
AOSHANG earloop is a Class II device made by Tianjin Aoshang Outdoor Equipment Co., Ltd., cleared under FDA 510(k) K210030 on 23 Apr 2021 and listed in FDA GUDID since 6 Aug 2021 (UDI-DI 06973532970049), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06973532970049 | Date6 Aug 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210030 | Date23 Apr 2021 | StatusActive |
Official records
- AccessGUDID record 06973532970049
- FDA 510(k) database K210030
Across registries
- FDA 510(k) K210030 decided 23 Apr 2021 Active
- FDA GUDID UDI-DI 06973532970049 listed 6 Aug 2021 Listed
Timeline
- Cleared FDA 510(k) K210030
- Listed FDA GUDID 06973532970049
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aoshang
- Generic name
- Surgical/medical face mask, single-use
- Model / reference
- earloop
- Primary DI / UDI-DI
- 06973532970049
- 510(k) Number
- FDA product code
- FXX
- GMDN term
- Surgical/medical face mask, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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