ULTRATHERA TECHNOLOGIES, INC.

FDA Device Registration & Listing · Colorado Springs, CO, US · Registration 3027406982

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
3027406982
FEI Number
3027406982
Entity Name
ULTRATHERA TECHNOLOGIES, INC.
City/State/Country
Colorado Springs, CO, US
Establishment Address
2 N Cascade Avenue, Suite 1320, Colorado Springs, CO 80903, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
UltraThera Technologies, Inc. (Owner Number: 10088173)
Owner / Operator Contact Address
2 N Cascade Avenue, Suite 1320, Colorado Springs, CO 80903, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K220231
PMA Number
N/A

All Registered Proprietary Names

GyroStim

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXV Apparatus, Vestibular Analysis Unknown Class U N/A 2023-06-06

Official Correspondent

Kevin Maher

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UltraThera Technologies, Inc.
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 3027406982. Last updated year: 2026. Please use registration number 3027406982 when referencing this establishment in official correspondence.
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