Oricle Hearing LLC

FDA Device Registration & Listing · San Diego, CA, US · Registration 3027202846

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
3027202846
FEI Number
3027202846
Entity Name
Oricle Hearing LLC
City/State/Country
San Diego, CA, US
Establishment Address
2400 Kettner Blvd Ste 238, San Diego, CA 92101, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Lifetime Well LLC (Owner Number: 10093120)
Owner / Operator Contact Address
2400 Kettner Blvd, Apt 238, San Diego, CA 92101, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QUH Self-Fitting Air-Conduction Hearing Aid, Over The Counter Ear, Nose, Throat Class 2 874.3325 2025-04-01

Official Correspondent

Tania Gray

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lifetime Well LLC
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 3027202846. Last updated year: 2026. Please use registration number 3027202846 when referencing this establishment in official correspondence.
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