Data / Medical devices / United States / The Snore Reliever Company
The Snore Reliever Company: FDA-registered device maker in Largo, FL, United States, 2 510(k) clearances
The Snore Reliever Company is registered with the FDA (registration 3008583502) in Largo, FL, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated January 14, 2021. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3008583502
- Address
- 8042 118th Ave N, Largo, FL, United States, 33773
- Owner or operator
- The Snore Reliever Company (10033460)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- August 18, 2010
- Registered through
- 2026
- Brand names listed
- Vital Sleep
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 2 | Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| January 14, 2021 | K201719 | Vital Sleep | LRK | Substantially Equivalent | The Snore Reliever Company, LLC | accessdata.fda.gov |
| January 13, 2010 | K092942 | VITAL SLEEP | LRK | Substantially Equivalent | The Snore Reliever Company, LLC | accessdata.fda.gov |
Compare with other makers
Updated January 14, 2021. 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.