PURESLEEP— 510(k) K113022

Name: FDA 510(k) clearance K113022
Creator: U.S. Food and Drug Administration
Published: 2012-06-11

Substantially Equivalent

Sleep Science Partners, Inc.

FDA 510(k) clearance K113022 for PURESLEEP, Substantially Equivalent on 2012-06-11. Applicant: Sleep Science Partners, Inc.. Device class: 2.

Clearance details

Applicant: Sleep Science Partners, Inc.
Product code: Code LRK
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 2011-10-11
Decision date: 2012-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Larkspur, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRK

view all

K262104 — Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)2026-08-27
K261912 — SnØreNegatØr2026-07-31
K261366 — Virtus2026-06-12
K261251 — Snorbliss® Anti-Snoring Device2026-06-11
K261134 — Dormiva Anti-Snoring Mouth Guard2026-05-14

More clearances from Sleep Science Partners, Inc.

view all

K190058 — PureSleep (OTC use)2019-04-11

Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.