ELIDAH

FDA Device Registration & Listing · Newtown, CT, US · Registration 3014915464

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014915464
FEI Number
3014915464
Entity Name
ELIDAH
City/State/Country
Newtown, CT, US
Establishment Address
31 Pecks Ln Ste 11, Newtown, CT 06470, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Elidah (Owner Number: 10059852)
Owner / Operator Contact Address
31 Pecks Ln Ste 11, Newtown, CT 06470, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K183585
PMA Number
N/A

All Registered Proprietary Names

Elitone for Men BetterSleep Compression Socks ELITONE URGE Elitone

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QAJ Cutaneous Electrode Stimulator For Urinary Incontinence Gastroenterology, Urology Class 2 876.5330 2026-04-10
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2022-12-01
QAJ Cutaneous Electrode Stimulator For Urinary Incontinence Gastroenterology, Urology Class 2 876.5330 2023-03-06
QAJ Cutaneous Electrode Stimulator For Urinary Incontinence Gastroenterology, Urology Class 2 876.5330 2019-02-28

Official Correspondent

Gloria Kolb

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Elidah
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014915464. Last updated year: 2026. Please use registration number 3014915464 when referencing this establishment in official correspondence.
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