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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 5 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens MidStream 6
FDA UDI
Class IIActive
Well at Walgreens 265335
FDA UDI
Class IActive
Walgreens 848898
FDA UDI
Class IActive
Walgreens 878287
FDA UDI
Class IActive
Walgreens 566682
FDA UDI
Class IActive
Walgreens 10002363
FDA UDI
Class IIActive
Walgreens 986721
FDA UDI
Class IActive
Walgreens 177299
FDA UDI
Class IActive
Well at Walgreens KD-2070
FDA UDI
Class IIActive
Walgreens 845575
FDA UDI
Class IIActive
Walgreens 277085
FDA UDI
Class IActive
Well at Walgreens 411435
FDA UDI
Class IIUnknown
Walgreens 795578
FDA UDI
Class IIActive
Walgreens 277080
FDA UDI
Class IActive
Walgreens 934777
FDA UDI
Class IIActive
Walgreens 985245
FDA UDI
Class IActive
Walgreens 864224
FDA UDI
Class IIActive
Walgreens 877132
FDA UDI
Class IIActive
Well at Walgreens 18704
FDA UDI
Class IIActive
Well at Walgreens KD-2150
FDA UDI
Class IIActive
Walgreens 444995
FDA UDI
Class IActive
Walgreens 992377
FDA UDI
Class IIActive
Walgreens 10170
FDA UDI
Class IIActive
Walgreens 688208
FDA UDI
Class IIActive
Walgreens 907805
FDA UDI
Class IIActive
Walgreens 109893
FDA UDI
Class IActive
Walgreens 705365
FDA UDI
Class IActive
Walgreens 876911
FDA UDI
Class IIActive
Walgreens 643451
FDA UDI
Class IIActive
Walgreens 785409
FDA UDI
Class IActive
Walgreens 244208
FDA UDI
NUnknown
Walgreens 277084
FDA UDI
Class IActive
Walgreens 110018
FDA UDI
Class IActive
Walgreens 170298
FDA UDI
Class IActive
Walgreens 153122
FDA UDI
Class IActive
Walgreens 972294
FDA UDI
Class IIActive
Well at Walgreens 995034
FDA UDI
Class IActive
Walgreens 385893
FDA UDI
Class IActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 985244
FDA UDI
Class IActive
Walgreens 884646
FDA UDI
Class IActive
Walgreens 795577
FDA UDI
Class IIActive
Well at Walgreens 307790
FDA UDI
Class IActive
Walgreens 586507
FDA UDI
Class IActive
Walgreens 214999
FDA UDI
Class IActive
Walgreens 220544
FDA UDI
UActive
Well at Walgreens CC14
FDA UDI
Class IIActive
Walgreens 676986
FDA UDI
Class IIActive
Walgreens 828147
FDA UDI
Class IIActive
Walgreens 214998
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

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