Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016181636

FEI Number

3016181636

Entity Name

QUICKSILVER SCIENTIFIC, INC.

City/State/Country

Louisville, CO, US

Establishment Address

1960 Cherry St., Louisville, CO 80027, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Quicksilver Scientific, Inc. (Owner Number: 10088445)

Owner / Operator Contact Address

1960 Cherry St., Louisville, CO 80027, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Quinton Action Plus Nasal Spray Quinton Daily Nasal Spray

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2023-07-24

Official Correspondent

Kimberly Stark

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Quicksilver Scientific, 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 3016181636. Last updated year: 2026. Please use registration number 3016181636 when referencing this establishment in official correspondence.