Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014469173

FEI Number

3014469173

Entity Name

CONTINENTAL MANUFACTURING CHEMIST

City/State/Country

Huxley, IA, US

Establishment Address

1501 BLUE SKY BLVD, Huxley, IA 50124, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Continental Manufacturing Chemist (Owner Number: 10082222)

Owner / Operator Contact Address

1501 BLUE SKY BLVD, Huxley, IA 50124, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SmartMouth® DryMouth Rehydrating Oral Rinse

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LFD	Saliva, Artificial	Unknown	Class U	N/A	2021-07-06

Official Correspondent

Jeremy Thede

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Continental Manufacturing Chemist

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 3014469173. Last updated year: 2026. Please use registration number 3014469173 when referencing this establishment in official correspondence.