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WALGREEN CO.

US

Last updated May 24, 2026

What WALGREEN CO. makes

The company produces unscented menstrual products including pads and tampons, as well as reusable tubular support bandages and compression stockings. It also offers rapid diagnostic kits for detecting human chorionic gonadotropin, adhesive strips for skin coverage, and reusable electronic medical devices like portable thermometers and sphygmomanometers.

The portfolio includes devices classified as Class I, Class II, and unclassified (U), all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates under U.S. regulatory oversight, adhering to applicable FDA requirements for medical devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Walgreen Co. manufacture?

Walgreen Co. produces a variety of medical devices, including unscented menstrual products like pads and tampons, reusable tubular support bandages, and compression stockings. It also offers diagnostic tools such as rapid kits for detecting human chorionic gonadotropin (HCG), skin-cover adhesive strips, and reusable electronic devices like portable thermometers and blood pressure monitors. These products serve both personal health and clinical applications.

Where is Walgreen Co. based, and how does that affect its regulatory oversight?

Walgreen Co. is based in the United States, which means its devices fall under FDA regulatory jurisdiction. The FDA classifies its products as Class I, Class II, or unclassified (U), depending on risk levels. Since the company operates domestically, its devices must comply with U.S. medical device regulations, including requirements for listing in the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries list Walgreen Co.’s medical devices?

Walgreen Co.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which is a central registry for tracking medical devices authorized in the U.S. This database helps ensure transparency and traceability of devices under FDA oversight, including those classified as Class I, Class II, or unclassified.

How are Walgreen Co.’s devices classified under FDA regulations?

Walgreen Co.’s devices are categorized into three classifications: Class I (low-risk devices like unscented menstrual products), Class II (moderate-risk items such as diagnostic kits or reusable bandages), and unclassified (U) devices, which may include specialized or emerging products. Classification determines regulatory controls, with Class I devices generally requiring less scrutiny than Class II, which may need performance standards or post-market surveillance.

What kinds of electronic medical devices does Walgreen Co. produce?

Walgreen Co. manufactures reusable electronic medical devices, including portable intermittent thermometers for measuring body temperature and automatic-inflation sphygmomanometers for blood pressure monitoring. These devices are designed for clinical or home use, adhering to FDA requirements for electronic medical instruments, which may include performance testing and safety standards depending on their classification.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
walgreens.com
LinkedIn
—
Facebook
—
Phone
1-800-925-4733
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
008965063

Catalogue (750)

Page 11 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 907765
FDA UDI
Class IIUnknown
Walgreens 313180
FDA UDI
Class IActive
Walgreen 875715
FDA UDI
Class IIActive
Walgreens 308032
FDA UDI
Class IActive
Walgreens N/A
FDA UDI
Class IIActive
Walgreens 369354
FDA UDI
Class IActive
Walgreens 621901
FDA UDI
Class IIActive
Well at Walgreens Digital Pregnancy Test
FDA UDI
Class IIUnknown
Walgreens 676988
FDA UDI
Class IIActive
Walgreens WG34012FN/8
FDA UDI
Class IIActive
Walgreens 344344
FDA UDI
Class IActive
Well at Walgreens WGNBPW-915
FDA UDI
Class IIActive
Walgreens 344345
FDA UDI
Class IActive
Walgreens 218257
FDA UDI
Class IActive
Walgreens 400578
FDA UDI
Class IActive
Walgreens 385894
FDA UDI
Class IActive
Walgreens 582769
FDA UDI
Class IIActive
Walgreens 767735
FDA UDI
Class IIActive
Walgreens 985243
FDA UDI
Class IActive
Walgreens 279022
FDA UDI
Class IActive
Walgreens 877133
FDA UDI
Class IIActive
Walgreens 881213
FDA UDI
UActive
Walgreens 01-0130
FDA UDI
Class IIActive
Well at Walgreens 275196
FDA UDI
Class IActive
Walgreens 159329
FDA UDI
Class IActive
Walgreens 170272
FDA UDI
Class IActive
Walgreens 2100-WGN
FDA UDI
Class IActive
Walgreens EP364
FDA UDI
Class IIActive
Walgreens 740186
FDA UDI
Class IIActive
Walgreens 314795
FDA UDI
Class IActive
Walgreens 308024
FDA UDI
Class IActive
Walgreens 993090
FDA UDI
Class IActive
Well at Walgreens 307751
FDA UDI
Class IActive
Walgreens 107277
FDA UDI
Class IActive
Walgreens 989833
FDA UDI
Class IActive
Walgreens 931934
FDA UDI
Class IActive
Walgreens 105728
FDA UDI
Class IIActive
Walgreens KD-1502
FDA UDI
Class IIActive
Walgreens 643489
FDA UDI
Class IIActive
Walgreens 877085
FDA UDI
Class IIActive
Walgreens 876979
FDA UDI
Class IActive
Walgreens 379016
FDA UDI
Class IActive
Walgreens 765426
FDA UDI
Class IIActive
Well at Walgreens 410974
FDA UDI
Class IIUnknown
Walgreens 787862
FDA UDI
Class IIActive
Well At Walgreens 973181
FDA UDI
Class IActive
Well at Walgreens 387157
FDA UDI
Class IActive
Walgreens 170271
FDA UDI
Class IActive
Walgreens 830535
FDA UDI
Class IActive
Well at Walgreens 995035
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Walgreen Co. has one FDA recall record initiated on November 23, 2011, which remains listed with a terminated status. The recall pertains to thermometers reported to have inaccurate readings.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Nov 23, 2011Z-0506-2012—terminated

The thermometers have been reported to have inaccurate readings