Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010120146

FEI Number

3010120146

Entity Name

ANSCHEL TECHNOLOGY INC.

City/State/Country

Rocky Point, NY, US

Establishment Address

1 Wildwood Rd, Rocky Point, NY 11778, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Anschel Technology Inc. (Owner Number: 10043846)

Owner / Operator Contact Address

1 wildwood road, Rocky Point, NY 11778, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K113785

PMA Number

N/A

All Registered Proprietary Names

SightSaver

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWE	Stimulator, Photic, Evoked Response	Neurology	Class 2	882.1890	2013-03-28

Official Correspondent

David Anschel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Anschel Technology 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 3010120146. Last updated year: 2026. Please use registration number 3010120146 when referencing this establishment in official correspondence.