Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1122810

FEI Number

1000123463

Entity Name

LOMBART INSTRUMENT

City/State/Country

NORFOLK, VA, US

Establishment Address

5358 ROBIN HOOD RD, NORFOLK, VA 23513, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

LOMBART INSTRUMENT (Owner Number: 9001340)

Owner / Operator Contact Address

5358 ROBIN HOOD RD., --, Norfolk, VA 23513, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Refractor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKN	Refractor, Manual, Non-Powered, Including Phoropter	Ophthalmic	Class 1	886.1770	2023-01-11

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LOMBART INSTRUMENT

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 1122810. Last updated year: 2026. Please use registration number 1122810 when referencing this establishment in official correspondence.