Elidah, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elidah, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Elitone for Men, ELITONE Urge Urinary Incontinence Device, Elitone Device
3
Total
3
Cleared
0
Denied
Elidah, Inc. has 3 FDA 510(k) cleared medical devices. Based in Monroe, US.
Latest FDA clearance: Jan 2026. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Elidah, Inc. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Elidah, Inc.
3 devices