Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3037699421

FEI Number

3037699421

Entity Name

RESOLA

City/State/Country

Idaho Falls, ID, US

Establishment Address

3814 Washington Pkwy, Idaho Falls, ID 83404, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Resola (Owner Number: 10093131)

Owner / Operator Contact Address

3814 Washington parkway, Idaho Falls, ID 83404, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Resola Care

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PKS	Exerciser, Non-Measuring For Stroke Rehabilitation	Physical Medicine	Class 1	890.5370	2025-04-03

Official Correspondent

Matt Stevens

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Resola

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 3037699421. Last updated year: 2026. Please use registration number 3037699421 when referencing this establishment in official correspondence.