THE ALGER COMPANY, INC.

FDA Device Registration & Listing · Lago Vista, TX, US · Registration 1625407

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1625407
FEI Number
1625407
Entity Name
THE ALGER COMPANY, INC.
City/State/Country
Lago Vista, TX, US
Establishment Address
320 FLIGHTLINE RD., Lago Vista, TX 78645, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
The Alger Company, INC. (Owner Number: 1625407)
Owner / Operator Contact Address
320 FLIGHTLINE RD., --, Lago Vista, TX 78645, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Algerbrush II

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHW Burr, Corneal, Battery Powered, Rust Ring Removal Ophthalmic Class 1 886.4070 2013-02-27

Official Correspondent

JOHN ALGER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Alger Company, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1625407. Last updated year: 2026. Please use registration number 1625407 when referencing this establishment in official correspondence.
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