MOTUS NOVA

FDA Device Registration & Listing · Atlanta, GA, US · Registration 3010898730

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
3010898730
FEI Number
3010898730
Entity Name
MOTUS NOVA
City/State/Country
Atlanta, GA, US
Establishment Address
2960 Brandywine Road, Suite 100, Atlanta, GA 30341, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Motus Nova (Owner Number: 10046915)
Owner / Operator Contact Address
3636 Habersham Rd, Suite 2406, Atlanta, GA 30305, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hand Mentor Foot Mentor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JFA Exerciser, Finger, Powered Physical Medicine Class 1 890.5410 2014-05-29
BXB Exerciser, Powered Physical Medicine Class 1 890.5380 2014-05-29

Official Correspondent

Stacy Kenworthy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Motus Nova
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 3010898730. Last updated year: 2026. Please use registration number 3010898730 when referencing this establishment in official correspondence.
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