Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1651723

FEI Number

3003200197

Entity Name

BTI Filtration

City/State/Country

Oklahoma City, OK, US

Establishment Address

4000 N Stiles Ave, Oklahoma City, OK 73105, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

4M VENTURES, INC. DBA BTI Filtration (Owner Number: 9072105)

Owner / Operator Contact Address

4000 N Stiles Ave, --, Oklahoma City, OK 73105, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K080703

PMA Number

N/A

All Registered Proprietary Names

BTI Carbon Exchange Service BTI Filtration Deionizer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FIP	Subsystem, Water Purification	Gastroenterology, Urology	Class 2	876.5665	2008-06-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

4M VENTURES, INC. DBA BTI Filtration

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K110578	Mar Cor Purification, Inc.	MILLENIUM HX PORTABLE REVERSE OSMOSIS WATER PURIFICATION SYSTEM	2011-05-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0004-05	Ameriwater Inc	2	AmeriWater Portable RO+, model numbers MR01 and MR02. The device is a reverse osmosis system for dialysis.

Similar Registrations

Registration Number	Establishment Name	Location
3010867648	NELSON ENVIRONMENTAL TECHNOLOGIES, INC.	Arlington, TX, US
2135346	CULLIGAN SOFT WATER SERVICE CO.	Minnetonka, MN, US
3015349756	DIALITY, INC.	Irvine, CA, US
3003550196	Veolia Water Treatment & Solutions	ARLINGTON, TX, US
9611824	FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH	SCHWEINFURT Bavaria, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1651723. Last updated year: 2026. Please use registration number 1651723 when referencing this establishment in official correspondence.