EMA 3D— 510(k) K232735

Substantially Equivalent

Ema Sleep Incorporated

FDA 510(k) clearance K232735 for EMA 3D, Substantially Equivalent on 2024-05-03. Applicant: Ema Sleep Incorporated.

Clearance details

Applicant: Ema Sleep Incorporated
Product code: Code LRK
Advisory panel: Dental
Date received: 2023-09-07
Decision date: 2024-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spicewood, TX, US

Download summary PDF View on FDA.gov ↗

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.