EnsoSleep 7.0
EnsoSleep 7.0 is a Class II device made by Ensodata, Inc., cleared under FDA 510(k) K210034 on 16 Jun 2021 and listed in FDA GUDID since 23 Feb 2024 (UDI-DI 00864458000414), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | Number00864458000414 | Date23 Feb 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210034 | Date16 Jun 2021 | StatusActive |
Official records
- AccessGUDID record 00864458000414
- FDA 510(k) database K210034
Across registries
- FDA 510(k) K210034 decided 16 Jun 2021 Active
- FDA GUDID UDI-DI 00864458000414 listed 23 Feb 2024 Listed
Timeline
- Cleared FDA 510(k) K210034
- Listed FDA GUDID 00864458000414
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EnsoSleep
- Generic name
- Sleep disorder interpretive software, professional-only
- Model / reference
- 7.0
- Primary DI / UDI-DI
- 00864458000414
- 510(k) Number
- FDA product code
- OLZ
- GMDN term
- Sleep disorder interpretive software, professional-only
- Device class
- Class II
- Regulation number
- 882.1400
- GUDID distribution status
- Not in Commercial Distribution
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