MYOHEALTH TECHNOLOGIES, LLC

FDA Device Registration & Listing · Portland, OR, US · Registration 3030686055

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
3030686055
FEI Number
3030686055
Entity Name
MYOHEALTH TECHNOLOGIES, LLC
City/State/Country
Portland, OR, US
Establishment Address
13765 NW Cornell Rd, Suite 150, Portland, OR 97229, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MyoHealth Technologies, LLC (Owner Number: 10090435)
Owner / Operator Contact Address
13765 NW Cornell Rd, Suite 150, Portland, OR 97229, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230548
PMA Number
N/A

All Registered Proprietary Names

Myoaligner Appliance

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQC Mouthguard, Prescription Unknown Class U N/A 2024-03-27
OCO Mouthguard, Migraine/Tension Headache Unknown Class U N/A 2024-03-27

Official Correspondent

Maryam Motlagh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MyoHealth Technologies, LLC
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 3030686055. Last updated year: 2026. Please use registration number 3030686055 when referencing this establishment in official correspondence.
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