TICKERWORKS, INC.

FDA Device Registration & Listing · Folsom, CA, US · Registration 3020772821

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
3020772821
FEI Number
3020772821
Entity Name
TICKERWORKS, INC.
City/State/Country
Folsom, CA, US
Establishment Address
1300 E Bidwell St Ste 110, Folsom, CA 95630, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
TICKERWORKS, INC. (Owner Number: 10083113)
Owner / Operator Contact Address
1300 E. Bidwell Street, Suite 105, Folsom, CA 95630, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TICKER Gentle Dose TROCHE POPS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2021-10-26

Official Correspondent

RAMIRO PEREZ

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TICKERWORKS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020772821. Last updated year: 2026. Please use registration number 3020772821 when referencing this establishment in official correspondence.
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