Spiro 710
Spiro 710 is a Class II device made by Fogless International AB, cleared under FDA 510(k) K122932 on 23 Dec 2013 and listed in FDA GUDID since 31 Mar 2018 (UDI-DI 07350061231121), active as of 23 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 | Number07350061231121 | Date31 Mar 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122932 | Date23 Dec 2013 | StatusActive |
Official records
- AccessGUDID record 07350061231121
- FDA 510(k) database K122932
Across registries
- FDA 510(k) K122932 decided 23 Dec 2013 Active
- FDA GUDID UDI-DI 07350061231121 listed 31 Mar 2018 Listed
Timeline
- Cleared FDA 510(k) K122932
- Listed FDA GUDID 07350061231121
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Spiro
- Generic name
- Tracheostomy tube speech valve
- Model / Ref / Catalog
- 710, 710-1K, 710-2K, 710-5K
- Primary DI / UDI-DI
- 07350061231121
- 510(k) Number
- FDA product code
- JOH
- GMDN term
- Tracheostomy tube speech valve
- Device class
- Class II
- Regulation number
- 868.5800
- GUDID distribution status
- In Commercial Distribution
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