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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 13 of 15
DeviceModel / ReferenceRegistriesClassStatus
Well at Walgreens 3056
FDA UDI
Class IIActive
Walgreens 049
FDA UDI
Class IIActive
Walgreens 989834
FDA UDI
Class IActive
Walgreens 723155
FDA UDI
Class IIActive
Walgreens 307758
FDA UDI
Class IActive
Well at Walgreens 319684
FDA UDI
Class IActive
Well at Walgreens 275201
FDA UDI
Class IActive
Well at Walgreens WGNBPA-940
FDA UDI
Class IIActive
Well at Walgreens 265338
FDA UDI
Class IActive
Walgreens 781995
FDA UDI
Class IActive
Well at Walgreens 944675
FDA UDI
Class IActive
Well at Walgreens 68-348
FDA UDI
Class IIActive
Walgreens 415498
FDA UDI
Class IActive
Well at Walgreens 411505
FDA UDI
Class IIUnknown
Walgreens 654882
FDA UDI
Class IIActive
Walgreens 486529
FDA UDI
NActive
Walgreens Multi-Use Digital MidStream 6
FDA UDI
Class IActive
Walgreens 124232
FDA UDI
Class IActive
Well at Walgreens 944671
FDA UDI
Class IActive
Walgreens 829878
FDA UDI
Class IActive
Walgreens 937761
FDA UDI
Class IIActive
Walgreens 05-113018
FDA UDI
Class IIActive
Walgreens 643495
FDA UDI
Class IIActive
Walgreens 221584
FDA UDI
Class IActive
Well at Walgreens One Step Pregnancy Test
FDA UDI
Class IIActive
Walgreens 350716
FDA UDI
Class IActive
Walgreens 547526
FDA UDI
NUnknown
Walgreens 853608
FDA UDI
Class IIActive
Walgreens 982837
FDA UDI
Class IActive
Well at Walgreens 189604
FDA UDI
Class IIUnknown
Walgreens 527931
FDA UDI
NActive
Walgreens 643496
FDA UDI
Class IIActive
Well at Walgreens 265334
FDA UDI
Class IActive
Walgreens 745309
FDA UDI
Class IIActive
Walgreens 749215
FDA UDI
Class IActive
Walgreens 437091
FDA UDI
Class IIActive
Walgreens 258743
FDA UDI
Class IUnknown
Well at Walgreens 18959
FDA UDI
Class IIActive
Walgreens 586508
FDA UDI
Class IActive
Walgreens 109892
FDA UDI
Class IActive
Well at Walgreens 317965
FDA UDI
Class IActive
Walgreens 733613
FDA UDI
Class IIActive
Walgreens 437181
FDA UDI
Class IIActive
Walgreens 630109
FDA UDI
UActive
Walgreens 985246
FDA UDI
Class IActive
Walgreens 984898
FDA UDI
Class IIActive
Walgreens 677259
FDA UDI
Class IIActive
Walgreens 296052
FDA UDI
Class IActive
Walgreens 10002378
FDA UDI
Class IIActive
Walgreens 219547
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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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