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Sign in to claim this brandWalmart Stores
US
Last updated May 23, 2026
What Walmart Stores makes
The company produces home-use glucose monitoring systems, including test strips and meters, along with single-use blood lancets for diabetic management. It also manufactures unscented menstrual products such as tampons and pads, as well as basic insulin syringes and autoinjector needles. Additional offerings include antimicrobial skin-cover adhesive strips and a basic electric toothbrush.
The portfolio includes devices classified as Class I, Class II, and unclassified (N/U), all listed in the FDA’s Unique Device Identifier (UDI) database. The company operates under U.S. regulatory oversight, with devices authorised for commercial distribution in the United States.
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 Walmart Stores manufacture?
Walmart Stores manufactures a range of medical devices primarily designed for home use. These include glucose monitoring systems (such as meters and test strips), single-use blood lancets, unscented menstrual products like tampons and pads, basic insulin syringes and autoinjector needles, antimicrobial skin-cover adhesive strips, and a basic electric toothbrush. These products cater to personal health and hygiene needs, with a focus on affordability and accessibility.
Where is Walmart Stores based, and under which regulatory framework do its devices operate?
Walmart Stores is based in the United States. Its medical devices are authorised for commercial distribution in the U.S. and fall under the regulatory oversight of the FDA. The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations.
Which regulatory registries or databases list Walmart Stores’ medical devices?
Walmart Stores’ medical devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized approach to identify medical devices throughout their distribution and helps ensure regulatory compliance, traceability, and transparency in the U.S. market.
How are Walmart Stores’ medical devices classified under U.S. regulations?
Walmart Stores’ devices are classified under three categories: Class I (generally low-risk devices requiring minimal regulation), Class II (moderate-risk devices with special controls), and unclassified (N/U). The classification depends on the device’s intended use and potential risk to patients, as determined by the FDA. For example, basic electric toothbrushes typically fall under Class I, while glucose monitoring systems may be Class II due to their role in managing chronic conditions.
What reasoning explains why some of Walmart Stores’ devices are unclassified (N/U)?
Some of Walmart Stores’ devices are marked as unclassified (N/U) because they may not have a specific FDA classification assigned yet or could be considered exempt from classification due to their minimal risk profile. Unclassified devices are still authorised for market distribution but may require additional documentation or compliance steps to demonstrate safety and effectiveness. The FDA periodically reviews and assigns classifications to devices as needed.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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Catalogue (369)
Page 4 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Equate | 681131436427 | FDA UDI | Class I | Active |
| equate Tampons | BWMPP36 | FDA UDI | Class II | Active |
| Equate | ZQG | FDA UDI | Class I | Active |
| Equate | 576025422 | FDA UDI | Class II | Active |
| Equate | W3431D | FDA UDI | Class II | Active |
| Ozark Trail Outdoor Equipment | 017276235890 | FDA UDI | N | Unknown |
| Member's Mark | 731365 | FDA UDI | Class II | Active |
| ReliOn | 194346270651 | FDA UDI | Class II | Active |
| ReliOn® Prime Blood Glucose Test Strips | 700025 | FDA UDI | Class II | Active |
| Equate | 4050957 | FDA UDI | Class I | Active |
| Insulin Syringes, 1mL 31G x 8MM | 328506 | FDA UDI | Class II | Active |
| ReliOn™ Premier Control Solution Level 1 | 780005 | FDA UDI | Class I | Active |
| Equate | 681131006750 | FDA UDI | Class I | Active |
| Equate | 681131006774 | FDA UDI | Class I | Active |
| Equate | 675151431 | FDA UDI | Class I | Active |
| Relion ULTRA-THIN Lancets | 01-0130 | FDA UDI | Class II | Active |
| Members Mark | 94213 | FDA UDI | Class II | Active |
| Equate | 563008516 | FDA UDI | Class II | Unknown |
| Equate | 110002-2 | FDA UDI | Class I | Active |
| ReliOn® micro Blood Glucose Monitoring System | 712001 | FDA UDI | Class II | Unknown |
| ReliOn™ Premier Blood Glucose Test Strips | 780050 / 780100 | FDA UDI | Class II | Active |
| Relion | 09556729001 | FDA UDI | Class II | Active |
| Equate | 681131006767 | FDA UDI | Class I | Unknown |
| Ozark Trail Outdoor Equipment | 017276235906 | FDA UDI | N | Unknown |
| Equate | 563004770 | FDA UDI | Class I | Active |
| Equate | 677296455 | FDA UDI | Class II | Active |
| Relion Pen Needles | 700001324 | FDA UDI | Class II | Active |
| Equate | 587326752 | FDA UDI | Class I | Active |
| Equate | 1 | FDA UDI | Class I | Active |
| Equate | 005635 | FDA UDI | Class II | Active |
| Equate | 581880438 | FDA UDI | Class II | Active |
| Equate | 70356WM | FDA UDI | U | Active |
| Equate Wrist Blood Pressure Monitor | 6500 Series | FDA UDI | Class II | Active |
| Members Mark | 990283306 | FDA UDI | Class II | Active |
| Equate | BPZ | FDA UDI | Class I | Active |
| Equate | 194346192083 | FDA UDI | U | Active |
| Member's Mark | 707001 | FDA UDI | Class II | Active |
| Equate | JP8191EQCLR200 | FDA UDI | Class I | Active |
| Equate | 269804 | FDA UDI | Class I | Active |
| ReliOn™ Premier BLU Basic Meter | 782001 | FDA UDI | Class II | Active |
| Equate | 630349 | FDA UDI | Class II | Active |
| Walmart Equate | Advanced Early Result Pregnancy Test | FDA UDI | Class II | Unknown |
| Equate | 422266 | FDA UDI | Class I | Active |
| Equate | 4000184 | FDA UDI | Class I | Active |
| equate | 681131161619 | FDA UDI | U | Active |
| ReliOn BP300W Wrist Blood Pressure Monitor | 6021RELN2 | FDA UDI | Class II | Active |
| Equate | EQ2119-UL | FDA UDI | Class I | Active |
| Equate | UVH | FDA UDI | Class I | Active |
| Ozark Trail Outdoor Equipment | 017276235876 | FDA UDI | N | Unknown |
| Equate | SC-110 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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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.
Walmart Stores has one FDA recall record initiated on February 26, 2014, which is listed with a terminated status. The recall involved fifteen pairs of prescription, safety glasses that did not comply with required industrial lens thickness specifications and lacked the mandatory OSHA manufacturer markings.
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 |
|---|---|---|---|---|
| Feb 26, 2014 | Z-1810-2014 | — | terminated | Fifteen pairs of prescription, safety glasses did not meet required, industrial lens thickness; nor did these glasses have the OSHA-required manufacturer markings. |