Sway Medical, Inc.

FDA Device Registration & Listing · Tulsa, OK, US · Registration 3010325634

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
3010325634
FEI Number
3010325634
Entity Name
Sway Medical, Inc.
City/State/Country
Tulsa, OK, US
Establishment Address
32 S. Lewis Ave, Tulsa, OK 74104, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Sway Medical, Inc (Owner Number: 10044583)
Owner / Operator Contact Address
32 S. Lewis Ave, Tulsa, OK 74104, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K121590
PMA Number
N/A

All Registered Proprietary Names

Sway Sports+ Sway Balance

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
POM Computerized Cognitive Assessment Aid For Concussion Neurology Class 2 882.1471 2025-03-03
LXV Apparatus, Vestibular Analysis Unknown Class U N/A 2013-06-28

Official Correspondent

Chase Curtiss

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sway Medical, Inc
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 3010325634. Last updated year: 2026. Please use registration number 3010325634 when referencing this establishment in official correspondence.
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