Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011521783

FEI Number

3011521783

Entity Name

Dymicron

City/State/Country

Orem, UT, US

Establishment Address

1186 S 1680 W, Orem, UT 84058, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

Dymicron, Inc. (Owner Number: 10048836)

Owner / Operator Contact Address

1186 S. 1680 W., Orem, UT 84058, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Triadyme-C

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MJO	Prosthesis, Intervertebral Disc	Unknown	Class 3	N/A	2015-03-09

Official Correspondent

David Carey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dymicron, 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 3011521783. Last updated year: 2026. Please use registration number 3011521783 when referencing this establishment in official correspondence.