Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011647051

FEI Number

3011647051

Entity Name

K PHARMACEUTICALS

City/State/Country

Phoenix, AZ, US

Establishment Address

5080 N 40th Street, Phoenix, AZ 85018, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

K Pharmaceuticals (Owner Number: 10086624)

Owner / Operator Contact Address

5080 N 40TH St, Phoenix, AZ 85018, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K051812

PMA Number

N/A

All Registered Proprietary Names

Aquoral Protective Oral Spray

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LFD	Saliva, Artificial	Unknown	Class U	N/A	2022-11-25

Official Correspondent

Christopher Di Lascia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

K Pharmaceuticals

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3014469173	CONTINENTAL MANUFACTURING CHEMIST	Huxley, IA, US
3007617180	CANADIAN DRY STORAGE LTD.	Richmond British Columbia, CA
3030049002	ROWPAR PHARMACEUTICALS INC.	Bridgewater, NJ, US
9613740	TRILLIUM HEALTH CARE PRODUCTS, INC.	BROCKVILLE Ontario, CA
3012943922	Fertin Canada Inc.	Langley British Columbia, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011647051. Last updated year: 2026. Please use registration number 3011647051 when referencing this establishment in official correspondence.