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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 1 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 124132
FDA UDI
Class IActive
Walgreens 998353
FDA UDI
Class IActive
Walgreens 346669
FDA UDI
Class IActive
Well at Walgreens 307748
FDA UDI
Class IActive
Walgreens 586403
FDA UDI
Class IActive
Walgreens 276740
FDA UDI
Class IActive
Well at Walgreens WGNBPW-910
FDA UDI
Class IIActive
Well at Walgreens 265341
FDA UDI
Class IActive
Well at Walgreens 377075
FDA UDI
Class IActive
Walgreens 230820
FDA UDI
Class IActive
Walgreens 156749
FDA UDI
Class IActive
Walgreens 935973
FDA UDI
Class IIActive
Walgreens 296463
FDA UDI
Class IActive
Walgreens 765430
FDA UDI
Class IIActive
Well at Walgreens 275193
FDA UDI
Class IActive
Walgreens 884645
FDA UDI
Class IUnknown
Walgreens 973078
FDA UDI
Class IActive
Well at Walgreens 275199
FDA UDI
Class IActive
Walgreen 107249
FDA UDI
Class IUnknown
Walgreens 295621
FDA UDI
Class IActive
Walgreens 295501
FDA UDI
Class IActive
Walgreens 400745
FDA UDI
Class IActive
Walgreens 172723
FDA UDI
Class IIActive
Walgreens 170293
FDA UDI
Class IActive
Walgreens 400577
FDA UDI
Class IActive
Walgreens Mess Free Lube 842712
FDA UDI
Class IIActive
Well at Walgreens 930448
FDA UDI
Class IIActive
Walgreens 603012
FDA UDI
Class IActive
Walgreens 937760
FDA UDI
Class IIActive
Walgreens 989835
FDA UDI
Class IActive
Walgreens 932196
FDA UDI
Class IActive
Walgreens 740216
FDA UDI
Class IIActive
Well at Walgreens 000886-912-583U
FDA UDI
Class IIUnknown
Walgreens 877902
FDA UDI
Class IActive
Walgreens 066
FDA UDI
Class IIActive
Walgreens 824632
FDA UDI
Class IIActive
Walgreens 642934
FDA UDI
Class IIActive
Walgreens 107282
FDA UDI
Class IActive
Walgreens 332420
FDA UDI
Class IActive
Walgreens 954487
FDA UDI
Class IUnknown
Walgreens 856466
FDA UDI
Class IIActive
Walgreens 460669
FDA UDI
Class IActive
Walgreens 781950
FDA UDI
Class IIActive
Walgreens QPZ-01
FDA UDI
Class IIActive
Walgreens 273085
FDA UDI
Class IIActive
Walgreens 829879
FDA UDI
Class IActive
Walgreens 10002364
FDA UDI
Class IIActive
Well at Walgreens FHT6C-WGFP-1_0
FDA UDI
Class IIActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 993095
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