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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 3 of 15
DeviceModel / ReferenceRegistriesClassStatus
Walgreens 272896
FDA UDI
Class IIActive
Walgreens 109881
FDA UDI
Class IActive
Well at Walgreens 129810
FDA UDI
Class IActive
walgreen's 886171
FDA UDI
UActive
Walgreens 1
FDA UDI
Class IIActive
Walgreens 156744
FDA UDI
Class IActive
Walgreens 740269
FDA UDI
Class IIActive
Walgreens 985247
FDA UDI
Class IActive
Walgreens 687380
FDA UDI
Class IIActive
Walgreens 379012
FDA UDI
Class IActive
Walgreens 762637
FDA UDI
Class IIActive
Well at Walgreens KI-8171L
FDA UDI
Class IIActive
Walgreens 740266
FDA UDI
Class IIActive
Walgreens 765431
FDA UDI
Class IIActive
Walgreens 170308
FDA UDI
Class IActive
Walgreens PF100-WAG
FDA UDI
Class IIActive
Walgreens 602993
FDA UDI
Class IActive
Walgreens 586337
FDA UDI
Class IActive
Walgreens 505807
FDA UDI
Class IActive
Walgreens 973669
FDA UDI
Class IActive
Walgreens 688652
FDA UDI
Class IIActive
Walgreens 272908
FDA UDI
Class IActive
Walgreens 150573
FDA UDI
Class IActive
Walgreens MOB951S.WLG
FDA UDI
Class IIActive
Walgreen's 142091
FDA UDI
UActive
Walgreens 931979
FDA UDI
Class IActive
Dentek 00015101203I2
FDA UDI
UActive
Walgreens 317956
FDA UDI
Class IActive
Well at Walgreens CC62
FDA UDI
Class IIUnknown
Walgreens 901365
FDA UDI
Class IActive
Walgreens 990443
FDA UDI
Class IActive
Walgreens 745308
FDA UDI
Class IIActive
Walgreens 307753
FDA UDI
Class IActive
Walgreens 888468
FDA UDI
Class IActive
Walgreens 877225
FDA UDI
UActive
Walgreens 156809
FDA UDI
Class IIActive
Walgreens Multi-Use Digital MidStream 6
FDA UDI
Class IActive
Walgreens 745607
FDA UDI
Class IIActive
Walgreens MidStream 6
FDA UDI
Class IIActive
Walgreens 733603
FDA UDI
Class IIActive
Walgreens Liquid Lubricant 407498 2 oz WAG Lube Liquid
FDA UDI
Class IIActive
Walgreens 170290
FDA UDI
Class IActive
Well at Walgreens MNV730-912-000U
FDA UDI
Class IIActive
Well at Walgreens 277302
FDA UDI
Class IActive
Well at Walgreens Early Result Pregnancy Test
FDA UDI
Class IIActive
Walgreens 277082
FDA UDI
Class IActive
Walgreens 920165
FDA UDI
Class IActive
Well at Walgreens 307759
FDA UDI
Class IActive
Lice Killing Shampoo 8 oz 986725
FDA UDI
Class IActive
Walgreens 170309
FDA UDI
Class IActive

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