ALDI, INC.

FDA Device Registration & Listing · BATAVIA, IL, US · Registration 1419898

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
1419898
FEI Number
1419898
Entity Name
ALDI, INC.
City/State/Country
BATAVIA, IL, US
Establishment Address
1200 NORTH KIRK RD., BATAVIA, IL 60510, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Aldi USA (Owner Number: 9005174)
Owner / Operator Contact Address
1200 NORTH KIRK RD., --, Batavia, IL 60510, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Visage Visage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2022-06-21
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2021-11-01
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2021-11-01
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2022-06-21

Official Correspondent

Victoria Williams

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aldi USA
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K010462 Avita Corporation AVITA PICCOLO/EXATO INFARED EAR THERMOMETER (TS2 & TS4 SERIES) 2001-04-11
K760421 Arbrook Mfg. Corp. THERMOMETER, SURVALENT-ELECTRONIC 1976-08-23
K813409 Yellow Springs Instrument Co., Inc. MODEL 2100 DUAL-DISPLAY TELE-THERMOMETER 1981-12-18
K830039 Science Development Corp. SDC RECTAL TEMP. PROBE PRODUCT #1020 1983-02-23
K842199 Sharp Electronics Corp. ELEC. DIGITAL THERMOMETER MT-20 & 30 1984-07-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0032-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1419898. Last updated year: 2026. Please use registration number 1419898 when referencing this establishment in official correspondence.
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