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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 4 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 980267
FDA UDI
Class IActive
Walgreen's 877249
FDA UDI
UActive
Walgreens 341871
FDA UDI
Class IActive
Walgreens 170311
FDA UDI
Class IActive
Walgreens 111642
FDA UDI
Class IActive
Walgreens 611091
FDA UDI
Class IActive
Walgreens Freeze Skin Tag Remover 625345
FDA UDI
Class IIActive
Walgreens 677258
FDA UDI
Class IIActive
Walgreens 597812
FDA UDI
Class IActive
Walgreens 592370
FDA UDI
Class IActive
Walgreens 380093
FDA UDI
Class IActive
Well at Walgreens One Step Pregnancy Test
FDA UDI
Class IIActive
Walgreens 272936
FDA UDI
Class IActive
Walgreens 274499
FDA UDI
NUnknown
Walgreens One Step Pregnancy Test
FDA UDI
Class IIActive
Walgreens BPAG1-20WAG (649485)
FDA UDI
Class IIActive
Well at Walgreens 899781
FDA UDI
Class IIActive
Walgreens 602992
FDA UDI
Class IActive
Well at Walgreens 659370
FDA UDI
Class IActive
Walgreens 296051
FDA UDI
Class IActive
Walgreens 732624
FDA UDI
Class IIActive
Walgreens 656702
FDA UDI
Class IIActive
Well at Walgreens 275202
FDA UDI
Class IUnknown
Walgreens 993094
FDA UDI
Class IActive
Walgreens 272943
FDA UDI
Class IActive
Walgreens 107267
FDA UDI
Class IActive
Walgreens 379015
FDA UDI
Class IActive
Walgreens 191338
FDA UDI
Class IIActive
Walgreens 643430
FDA UDI
Class IIActive
Walgreens 890568
FDA UDI
Class IIActive
Walgreens 954486
FDA UDI
Class IActive
Walgreens Early Result Pregnancy Test
FDA UDI
Class IIActive
Walgreens 166910
FDA UDI
Class IIActive
Well at Walgreens 786610
FDA UDI
Class IActive
Walgreens 505802
FDA UDI
Class IActive
Walgreens 871026
FDA UDI
Class IActive
Walgreens 823376
FDA UDI
UActive
Walgreens 170299
FDA UDI
Class IActive
Walgreens 158981
FDA UDI
Class IActive
Walgreens 787890
FDA UDI
Class IIActive
Walgreens 100% Organic cotton with plastic applicator - REGULAR
FDA UDI
Class IIActive
Walgreens 350553
FDA UDI
Class IActive
Walgreens 341625
FDA UDI
Class IActive
Walgreens 554819
FDA UDI
Class IIActive
Walgreens 369358
FDA UDI
Class IActive
Walgreens 984899
FDA UDI
Class IIActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 407160
FDA UDI
Class IActive
Well at Walgreens 80029
FDA UDI
Class IIActive
Walgreens 317968
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