Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013316299

FEI Number

3013316299

Entity Name

Newton, INC.

City/State/Country

Coppell, TX, US

Establishment Address

1234 Lakeshore Drive, Suite 200, Coppell, TX 75019, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Newton Inc. (Owner Number: 10055367)

Owner / Operator Contact Address

1234 Lakeshore Drive, Suite 200, Coppell, TX 75019, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HJR	Stereoscope, Battery-Powered	Ophthalmic	Class 1	886.1870	2017-07-13
HJQ	Stereoscope, Ac-Powered	Ophthalmic	Class 1	886.1870	2017-07-13
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2017-07-18

Official Correspondent

Davis Corley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Newton 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 3013316299. Last updated year: 2026. Please use registration number 3013316299 when referencing this establishment in official correspondence.