Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 12 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 277086
FDA UDI
Class IActive
Walgreens 643428
FDA UDI
Class IIActive
Walgreens 220550
FDA UDI
UActive
Walgreens 953614
FDA UDI
Class IIActive
Walgreens 937877
FDA UDI
Class IActive
Walgreens 765423
FDA UDI
Class IIActive
Walgreen's 877283
FDA UDI
UActive
Walgreens 689453
FDA UDI
Class IIActive
Walgreens 853601
FDA UDI
Class IIActive
Walgreens 170289
FDA UDI
Class IActive
Well at Walgreens 944681
FDA UDI
Class IActive
Walgreens 811872
FDA UDI
Class IActive
Well at Walgreens 899709
FDA UDI
Class IIActive
Walgreens 597947
FDA UDI
Class IIActive
Well at Walgreens 265344
FDA UDI
Class IActive
Walgreens 584234
FDA UDI
Class IIActive
Walgreens 107266
FDA UDI
Class IActive
Walgreens 10002368
FDA UDI
Class IIActive
Walgreens 351587
FDA UDI
Class IIActive
Walgreens 901364
FDA UDI
Class IActive
Well at Walgreens 935768
FDA UDI
Class IIActive
Well at Walgreens Early Result Pregnancy Test
FDA UDI
Class IIActive
Walgreens 954484
FDA UDI
Class IActive
Walgreens 954489
FDA UDI
Class IUnknown
Walgreens 740699
FDA UDI
Class IActive
Walgreens 877289
FDA UDI
Class IIActive
Walgreens 876909
FDA UDI
Class IIActive
Walgreens 170279
FDA UDI
Class IActive
Walgreens 443529
FDA UDI
Class IIActive
Walgreens 150014
FDA UDI
Class IActive
Walgreens 611179
FDA UDI
Class IActive
Walgreens 932449
FDA UDI
Class IActive
Walgreens 760847
FDA UDI
Class IActive
Walgreens 276735
FDA UDI
Class IActive
Walgreens 369355
FDA UDI
Class IActive
Walgreens 725823
FDA UDI
Class IActive
Walgreens Bite Relief
FDA UDI
Class IIActive
Walgreens 170274
FDA UDI
Class IActive
Walgreens 344343
FDA UDI
Class IActive
Walgreens 153123
FDA UDI
Class IActive
Walgreens 795607
FDA UDI
Class IIActive
Walgreens 277304
FDA UDI
Class IActive
Well at Walgreens UPG2NWG-FP-1_0
FDA UDI
Class IIUnknown
Walgreens 313177
FDA UDI
Class IActive
Well at Walgreens 307743
FDA UDI
Class IActive
Walgreens 954779
FDA UDI
Class IIActive
Walgreens 256026
FDA UDI
Class IIActive
Well at Walgreens FHT5AWG-FP-1_0
FDA UDI
Class IIActive
Walgreens 332419
FDA UDI
Class IActive
Walgreens 100% Organic cotton with plastic applicator - SUPER
FDA UDI
Class IIActive

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