Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002968900

FEI Number

3002968900

Entity Name

OCUTECH, INC.

City/State/Country

Chapel Hill, NC, US

Establishment Address

105 Conner Dr Ste 2105, Chapel Hill, NC 27514, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ocutech, Inc. (Owner Number: 10039892)

Owner / Operator Contact Address

105 Conner Drive, Ste 2105, Chapel Hill, NC 27514, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SideSight(TM)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HPG	Aid, Vision, Electronic, Battery-Powered	Ophthalmic	Class 1	886.5900	2023-08-04

Official Correspondent

Henry Greene

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ocutech, 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 3002968900. Last updated year: 2026. Please use registration number 3002968900 when referencing this establishment in official correspondence.