AUTONOMYO USA

FDA Device Registration & Listing · Huntingdon Valley, PA, US · Registration 3043667885

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
3043667885
FEI Number
3043667885
Entity Name
AUTONOMYO USA
City/State/Country
Huntingdon Valley, PA, US
Establishment Address
2617 Huntingdon Pike, Huntingdon Valley, PA 19006, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Autonomyo USA (Owner Number: 10095332)
Owner / Operator Contact Address
2617 Huntingdon Pike, Huntingdon Valley, PA 19006, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Skywalk

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 2026-02-27

Official Correspondent

Rene Trost

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Autonomyo USA
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043667885. Last updated year: 2026. Please use registration number 3043667885 when referencing this establishment in official correspondence.
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