Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017723982

FEI Number

3017723982

Entity Name

OpenMotion AI, Inc.

City/State/Country

Dripping Springs, TX, US

Establishment Address

15431 Fitzhugh Rd Ste 208, Dripping Springs, TX 78620, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

OpenMotion AI, Inc. (Owner Number: 10093461)

Owner / Operator Contact Address

15431 Fitzhugh Rd. Unit 208, Dripping Springs, TX 78620, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Digital Twin BioSleeve OpenMotionAI MotionSleeve KineticOS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2025-05-19

Official Correspondent

Christopher Hall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OpenMotion AI, Inc.

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

View Entity Profile →

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3022375812	BIOINTERACTIVE TECHNOLOGIES INC.	Vancouver British Columbia, CA
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017723982. Last updated year: 2026. Please use registration number 3017723982 when referencing this establishment in official correspondence.