Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015193527

FEI Number

3015193527

Entity Name

KELLIDA INC

City/State/Country

Atlanta, GA, US

Establishment Address

4035 Whitewater Creek Rd Nw, Atlanta, GA 30327, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kellida Inc (Owner Number: 10059595)

Owner / Operator Contact Address

3715 Northside Parkway NW, 400 Northcreek, STE 150, Atlanta, GA 30327, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

miRing

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQG	Adaptor, Holder, Syringe	Physical Medicine	Class 1	890.5050	2019-02-01

Official Correspondent

Virginia Keating

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kellida Inc

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 3015193527. Last updated year: 2026. Please use registration number 3015193527 when referencing this establishment in official correspondence.