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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 6 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 276743
FDA UDI
Class IActive
Well at Walgreens MDPS100
FDA UDI
Class IIActive
Walgreens 287211
FDA UDI
Class IActive
Walgreens 554800
FDA UDI
Class IActive
Walgreens 604310
FDA UDI
Class IActive
Walgreens 451624
FDA UDI
Class IActive
Walgreens 797626
FDA UDI
Class IIActive
Walgreens 830427
FDA UDI
Class IActive
Walgreens 170310
FDA UDI
Class IActive
Walgreens 765422
FDA UDI
Class IIActive
Walgreens 317957
FDA UDI
Class IActive
Walgreens 836068
FDA UDI
Class IIActive
Walgreens MHP819S
FDA UDI
Class IIActive
Walgreens N/A
FDA UDI
Class IIActive
Walgreens 864133
FDA UDI
Class IIActive
Well at Walgreens 265339
FDA UDI
Class IActive
Walgreens 049
FDA UDI
Class IIActive
Walgreens 826300
FDA UDI
Class IIActive
Walgreens 158976
FDA UDI
Class IActive
Walgreens 940856
FDA UDI
UActive
Walgreens WALG INFRARED NON-CONTACT THERM
FDA UDI
Class IIActive
Walgreens 349123
FDA UDI
Class IActive
Walgreens 444936
FDA UDI
Class IActive
Walgreens 107251
FDA UDI
Class IUnknown
Lancets 01-0128
FDA UDI
Class IIActive
Walgreens 890625
FDA UDI
Class IIActive
Walgreens 311917136295
FDA UDI
Class IActive
Walgreens 276739
FDA UDI
Class IActive
Walgreens 931589
FDA UDI
Class IActive
Walgreens 985241
FDA UDI
Class IActive
Well at Walgreens 317966
FDA UDI
Class IActive
Walgreens 277087
FDA UDI
Class IActive
Walgreens 156829
FDA UDI
Class IIActive
Walgreens WG14012FN/8
FDA UDI
Class IIActive
Well at Walgreens 411505
FDA UDI
Class IIUnknown
Walgreens 548304
FDA UDI
Class IActive
Well at Walgreens 265333
FDA UDI
Class IActive
Walgreens 748000
FDA UDI
Class IActive
Walgreens 158977
FDA UDI
Class IUnknown
Well at Walgreens 449724
FDA UDI
Class IActive
Walgreens 826766
FDA UDI
Class IActive
Walgreens 10170
FDA UDI
Class IIActive
Walgreens 107279
FDA UDI
Class IActive
Walgreens 869513
FDA UDI
Class IIActive
Walgreens 845887
FDA UDI
Class IIActive
Walgreens 369356
FDA UDI
Class IActive
Well at Walgreens FDES105B Body Pads (P105B-2)
FDA UDI
Class IIActive
Walgreens 319054
FDA UDI
Class IActive
Well at Walgreens WRX320926
FDA UDI
Class IIUnknown
Well at Walgreens FDES105B
FDA UDI
Class IIActive

Related Companies

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Importers

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Authorities

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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