Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004461389

FEI Number

3004461389

Entity Name

AQUA CREEK PRODUCTS

City/State/Country

Missoula, MT, US

Establishment Address

9889 Garrymore Ln, Missoula, MT 59808, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Aqua Creek Products (Owner Number: 10027406)

Owner / Operator Contact Address

9889 Garrymore Lane, Missoula, MT 59808, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Revolution XL Portable Pro 2 Nebula Ranger 2 Pro Pool Lift Pro Spa 40 Lift Spa Lift EZ Pool Lift Portable Pro Pool Lift Revolution Lift Pro Spa 60 Lift Power EZ Lift Neptune Scout Excel Admiral Mighty 400 Mighty 600 Mighty Voyager

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2008-11-05

Official Correspondent

Krystal Guilhemotonia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aqua Creek Products

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004461389. Last updated year: 2026. Please use registration number 3004461389 when referencing this establishment in official correspondence.