MySleepDash— 510(k) K252338
Substantially EquivalentSomnetics International, Inc. (Dba Transcend Inc)
FDA 510(k) clearance K252338 for MySleepDash, Substantially Equivalent on 2026-04-17. Applicant: Somnetics International, Inc. (Dba Transcend Inc).
Clearance details
- Applicant
- Somnetics International, Inc. (Dba Transcend Inc)
- Product code
- Code BZD
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fridley, MN, US
Adverse events under product code BZD
product code BZD- Death
- 4,440
- Injury
- 53,099
- Malfunction
- 213,222
- Other
- 17
- Total
- 270,778
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.