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Data / Medical devices / United States / Snorelessnow LLC

Snorelessnow LLC: FDA-registered device maker in Mount Airy, MD, United States, 1 510(k) clearance

Snorelessnow LLC is registered with the FDA (registration 3027579589) in Mount Airy, MD, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 16, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3027579589
Address
401 Center St STE 104, Mount Airy, MD, United States, 21771
Owner or operator
SnoreLessNow LLC (10088217)
Roles
Repackager or relabeler
First device listed
July 28, 2023
Registered through
2026
Brand names listed
Airflow Clip, Anti-Snore Mouth Guard+, Somnofit-S Anti-Snore Mouth Guard+

Devices it lists

DeviceProduct codeClassRoleSource
Device, Anti-SnoringLRK2Repackager or relabeleraccessdata.fda.gov
Dilator, NasalLWF1Repackager or relabeleraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 16, 2024K231138Aniti-Snore Mouthguard+LRKSubstantially EquivalentOscimed SAaccessdata.fda.gov

Compare with other makers

Updated January 16, 2024. 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.