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Sign in to claim this brandWALGREEN 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
- —
- —
- [email protected]
- Phone
- 1-800-925-4733
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 008965063
Catalogue (750)
Page 15 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Walgreens | 272935 | FDA UDI | U | Active |
| Walgreens | Early Result Pregnancy Test | FDA UDI | Class II | Active |
| Well at Walgreens | 407763 | FDA UDI | Class II | Unknown |
| Walgreens | 158980 | FDA UDI | Class I | Active |
| Walgreens | 986727 | FDA UDI | Class I | Active |
| Walgreens | 116420 | FDA UDI | Class I | Active |
| Walgreens | mhp711s | FDA UDI | Class II | Active |
| Walgreens | 313178 | FDA UDI | Class I | Active |
| Walgreens | 066 | FDA UDI | Class II | Active |
| Walgreens | 276509 | FDA UDI | Class II | Active |
| Walgreens | 218632 | FDA UDI | Class II | Active |
| Walgreens | 274636 | FDA UDI | Class II | Active |
| Walgreens | 273080 | FDA UDI | Class II | Active |
| Walgreens | 839164 | FDA UDI | N | Active |
| Walgreens | 875421 | FDA UDI | Class I | Active |
| Walgreens | 747999 | FDA UDI | Class I | Active |
| Well at Walgreens | 68-370 | FDA UDI | Class II | Active |
| Walgreens | Digital & One Step Pregnancy Tests | FDA UDI | Class II | Unknown |
| Walgreens | 603476 | FDA UDI | Class I | Active |
| Well at Walgreens | 265340 | FDA UDI | Class I | Active |
| Walgreens | 982718 | FDA UDI | Class I | Active |
| Well at Walgreens | One Step Pregnancy Test | FDA UDI | Class II | Active |
| Walgreens | 603024 | FDA UDI | Class II | Active |
| Walgreens | 191340 | FDA UDI | Class II | Active |
| Walgreens | 603912 | FDA UDI | Class I | Active |
| Walgreens | 129843 | FDA UDI | Class II | Active |
| Walgreens | 200791 | FDA UDI | U | Active |
| Walgreens | MidStream 6 | FDA UDI | Class II | Active |
| Well at Walgreens | 995037 | FDA UDI | Class I | Active |
| Walgreens | 133278 | FDA UDI | Class I | Unknown |
| Walgreens | 277081 | FDA UDI | Class I | Active |
| Well at Walgreens | 944673 | FDA UDI | Class I | Active |
| Walgreens | 400569 | FDA UDI | Class I | Active |
| Walgreens | 985363 | FDA UDI | Class I | Active |
| Rapid Seal | 871180 | FDA UDI | U | Active |
| Well at Walgreens | 000886-912-000U | FDA UDI | Class II | Active |
| Well at Walgreens | MD300CN350R | FDA UDI | Class II | Active |
| Well at Walgreens | OxyWatch C20 | FDA UDI | Class II | Active |
| Well at Walgreens | 384673 | FDA UDI | Class II | Unknown |
| Well at Walgreens | KD-113 | FDA UDI | Class II | Active |
| Well at Walgreens | 275210 | FDA UDI | Class I | Active |
| Well at Walgreens | 413843 | FDA UDI | Class II | Unknown |
| Well at Walgreens | 155719 | FDA UDI | Class II | Active |
| Well at Walgreens | 307762 | FDA UDI | Class I | Active |
| Well at Walgreens | 18719 | FDA UDI | Class II | Active |
| Well at Walgreens | FDES150B Back Pads (P105B-1) | FDA UDI | Class II | Active |
| Well at Walgreens | 382865 | FDA UDI | Class I | Active |
| Well at Walgreens | 900371 | FDA UDI | Class II | Active |
| Well at Walgreens | 265337 | FDA UDI | Class I | Active |
| Sunglasses | K920169 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
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Importers
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 23, 2011 | Z-0506-2012 | — | terminated | The thermometers have been reported to have inaccurate readings |