JOINTSMART LLC

FDA Device Registration & Listing · Boyne City, MI, US · Registration 3036496902

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3036496902
FEI Number
3036496902
Entity Name
JOINTSMART LLC
City/State/Country
Boyne City, MI, US
Establishment Address
1675 S M 75, Boyne City, MI 49712, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
JointSmart LLC (Owner Number: 10092760)
Owner / Operator Contact Address
1675 S M75, Boyne City, MI 49712, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Shoulderreliever

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2025-02-14

Official Correspondent

Robert Swartz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JointSmart 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 3036496902. Last updated year: 2026. Please use registration number 3036496902 when referencing this establishment in official correspondence.
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