Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021530119

FEI Number

3021530119

Entity Name

Restorear Devices LLC

City/State/Country

Bozeman, MT, US

Establishment Address

613 Nikles Drive Suite 102, Bozeman, MT 59715, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Restorear Devices LLC (Owner Number: 10088764)

Owner / Operator Contact Address

613 Nikles Drive Suite 102, Bozeman, MT 59715, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ReBound Aero ReBound ReBound Lite

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2023-10-09

Official Correspondent

Curtis King

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Restorear Devices LLC

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 3021530119. Last updated year: 2026. Please use registration number 3021530119 when referencing this establishment in official correspondence.