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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 14 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 156825
FDA UDI
Class IIActive
Walgreens 740226
FDA UDI
Class IIActive
Walgreens 159325
FDA UDI
Class IActive
Walgreens 245340
FDA UDI
Class IActive
Walgreens 901363
FDA UDI
Class IActive
Walgreens 153127
FDA UDI
Class IActive
Walgreens 643462
FDA UDI
Class IIActive
Walgreens 778551
FDA UDI
Class IActive
Walgreens 439488
FDA UDI
Class IIActive
Walgreens 276736
FDA UDI
Class IActive
Well at Walgreens WGNBPA-950
FDA UDI
Class IIUnknown
Walgreens 643429
FDA UDI
Class IIActive
Walgreens 149828
FDA UDI
Class IActive
Walgreens 586505
FDA UDI
Class IActive
Walgreens 313179
FDA UDI
Class IActive
Walgreens 103761
FDA UDI
Class IIActive
Walgreens 107378
FDA UDI
Class IActive
Walgreens 310077
FDA UDI
Class IIActive
Walgreens 170291
FDA UDI
Class IActive
Walgreens 295675
FDA UDI
Class IActive
Walgreens 973079
FDA UDI
Class IActive
Walgreens 677257
FDA UDI
Class IIActive
Walgreens 274617
FDA UDI
Class IIActive
Walgreens 977960
FDA UDI
Class IActive
Walgreens 369359
FDA UDI
Class IActive
Walgreens KD-195-1
FDA UDI
Class IIActive
Walgreens 689301
FDA UDI
Class IIActive
Walgreens 10002373
FDA UDI
Class IIActive
Walgreens 10170
FDA UDI
Class IIActive
Walgreens 868912
FDA UDI
Class IIActive
Walgreens 170277
FDA UDI
Class IActive
Walgreens 901366
FDA UDI
Class IActive
Walgreens 219545
FDA UDI
Class IIActive
Walgreens 7W926
FDA UDI
Class IIActive
Walgreens 281132
FDA UDI
Class IIActive
Walgreens LT1102B
FDA UDI
Class IIActive
Well at Walgreens 000886-912-310U
FDA UDI
Class IIUnknown
Walgreens 540342
FDA UDI
Class IActive
Walgreens 795583
FDA UDI
Class IIActive
Walgreens 848748
FDA UDI
Class IActive
Walgreens 451299
FDA UDI
Class IActive
Walgreens 857779
FDA UDI
Class IActive
Walgreens 709864
FDA UDI
Class IActive
Walgreens 332421
FDA UDI
Class IActive
Walgreens 742401
FDA UDI
Class IIActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 878284
FDA UDI
Class IActive
Walgreens 735168
FDA UDI
Class IActive
Well at Walgreens 275204
FDA UDI
Class IActive
Well at Walgreens WGNBPW-930BT
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