Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3041847859

FEI Number

3041847859

Entity Name

HUMAN MOTION TECHNOLOGIES LLC

City/State/Country

Pittsburgh, PA, US

Establishment Address

630 William Pitt Way, Building A2, Pittsburgh, PA 15238, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Human Motion Technologies LLC (Owner Number: 10094262)

Owner / Operator Contact Address

630 William Pitt Way, Building A2, Pittsburgh, PA 15238, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Clinical Caplex® System with PRO-002

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISH	Component, External, Limb, Ankle/Foot	Physical Medicine	Class 1	890.3420	2025-11-20

Official Correspondent

Joshua Caputo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Human Motion Technologies 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 3041847859. Last updated year: 2026. Please use registration number 3041847859 when referencing this establishment in official correspondence.