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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 8 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 656620
FDA UDI
Class IIActive
Walgreens 505288
FDA UDI
NActive
Walgreens 170297
FDA UDI
Class IActive
Walgreen's 877224
FDA UDI
UActive
Walgreens 876905
FDA UDI
Class IIActive
Walgreens 104461
FDA UDI
Class IIActive
Walgreens 505377
FDA UDI
Class IIActive
Walgreens 256278
FDA UDI
NActive
Well at Walgreens 307742
FDA UDI
Class IActive
Walgreens 742985
FDA UDI
Class IIActive
Walgreens 642935
FDA UDI
Class IIActive
Walgreens 654878
FDA UDI
Class IIActive
Walgreens 203666
FDA UDI
Class IActive
Walgreens 993092
FDA UDI
Class IActive
Walgreens 767732
FDA UDI
Class IIActive
Well at Walgreens 255914
FDA UDI
Class IActive
Walgreens Certainty 436138
FDA UDI
Class IActive
Walgreens 937882
FDA UDI
Class IActive
Walgreens 998354
FDA UDI
Class IActive
Walgreens 170302
FDA UDI
Class IActive
Walgreens 396767
FDA UDI
Class IActive
Walgreen's 877281
FDA UDI
UActive
Well at Walgreens 000535-912-001U
FDA UDI
Class IIActive
Walgreens 377165
FDA UDI
Class IUnknown
Walgreens 993024
FDA UDI
Class IActive
Walgreens 901361
FDA UDI
Class IActive
Walgreens 01-0130
FDA UDI
Class IIActive
Walgreens 158979
FDA UDI
Class IActive
Walgreens 853612
FDA UDI
Class IIActive
Walgreens 156827
FDA UDI
Class IIActive
Walgreens WG24012FN/8
FDA UDI
Class IIActive
Walgreens 10170
FDA UDI
Class IIActive
Walgreens 170280
FDA UDI
Class IActive
Well At Walgreens 157670
FDA UDI
Class IActive
Well at Walgreens 307782
FDA UDI
Class IActive
Well at Walgreens 384674
FDA UDI
Class IActive
Walgreens 901359
FDA UDI
Class IActive
Walgreens 170300
FDA UDI
Class IActive
Walgreens 381506
FDA UDI
Class IActive
Walgreens 972813
FDA UDI
Class IActive
Walgreens 170294
FDA UDI
Class IActive
Walgreens 985242
FDA UDI
Class IActive
Walgreens 10170
FDA UDI
Class IIActive
Walgreens 10002377
FDA UDI
Class IIActive
Walgreens 878534
FDA UDI
Class IActive
Walgreens 817222
FDA UDI
Class IActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 934767
FDA UDI
Class IActive
Walgreens 973093
FDA UDI
Class IActive
Walgreens 296464
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