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Sign in to claim this brandTARGET CORPORATION
US
Last updated May 24, 2026
What TARGET CORPORATION makes
Target Corporation manufactures unscented menstrual tampons and pads, single-use earplugs, and multi-purpose soft contact lens solutions designed for eye care. Their portfolio also includes non-antimicrobial adhesive strips, intermittent electronic thermometers for patient use, reusable non-latex pressure bandages, and electric heating pads for localized body warmth.
The company’s devices are regulated under FDA classification as Class I, Class II, or exempt (N/U), with all listed in the FDA’s Unique Device Identifier (UDI) database. Target Corporation is headquartered 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 Target Corporation manufacture?
Target Corporation produces a variety of medical devices including unscented menstrual tampons and pads, single-use earplugs, and multi-purpose soft contact lens solutions. Their portfolio also covers non-antimicrobial skin-cover adhesive strips, intermittent electronic patient thermometers, reusable non-latex pressure bandages, and electric heating pads for localized warmth. These devices serve personal health, hygiene, and comfort needs.
Where is Target Corporation based, and how does that affect its devices?
Target Corporation is headquartered in the United States, which means its devices fall under FDA regulation. The FDA classifies their products as either Class I (low risk, general controls), Class II (moderate risk, requires special controls), or exempt (N/U), depending on their intended use and potential risks. This classification determines the regulatory pathway for each device.
Which regulatory registries list Target Corporation’s devices?
Target Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability for regulatory and market surveillance purposes.
How are Target Corporation’s devices classified by the FDA?
The FDA classifies Target Corporation’s devices into three categories: Class I (for low-risk items like reusable pressure bandages), Class II (for moderate-risk items such as intermittent electronic thermometers), or exempt (N/U) for devices like unscented menstrual products that meet specific criteria for minimal risk. Classification depends on factors like intended use, potential harm, and regulatory history.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- sunwin-sh.com
- —
- —
- [email protected]
- Phone
- 216 036 0238
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 006961700
Catalogue (183)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Up & Up | 245-09-0095 | FDA UDI | U | Active |
| Up&Up Tampons | 245-04-0370 | FDA UDI | Class II | Active |
| Up & Up | 094-06-0018 | FDA UDI | Class II | Active |
| Up & Up | 722-TPL-000U | FDA UDI | Class II | Active |
| Up&Up Tampons | 245-04-0408 | FDA UDI | Class II | Active |
| Up & Up | 094-06-0014 | FDA UDI | Class II | Active |
| Up & Up | 245-09-0062 | FDA UDI | U | Active |
| Up&Up | 245071573 | FDA UDI | Class I | Active |
| Up&Up | 245070700 | FDA UDI | Class I | Active |
| Up&Up | 245071145 | FDA UDI | Class I | Active |
| Up & Up | 0245-09-0145 | FDA UDI | U | Active |
| up & up | 245040188 | FDA UDI | Class I | Active |
| Up & Up | DT003 | FDA UDI | Class II | Active |
| Up&Up | 245-07-0707 | FDA UDI | Class I | Active |
| up & up rigid gas permeable contact lens cleaner | 630380 | FDA UDI | N/A | Active |
| Up & Up | PC40-TG | FDA UDI | Class II | Active |
| up & up | 245040457 | FDA UDI | Class I | Active |
| Up&Up Tampons | 245-04-0387 | FDA UDI | Class II | Active |
| Up&Up | 2B9 | FDA UDI | Class I | Active |
| Up & Up | Early-Result Pregnancy Test | FDA UDI | Class II | Unknown |
| Up & Up | 0245-09-0095 | FDA UDI | U | Active |
| Up & Up | 0245-09-0062 | FDA UDI | U | Active |
| Up&Up | 094-06-0014 | FDA UDI | Class II | Active |
| Up & Up | ET003 | FDA UDI | Class II | Active |
| Up & Up | 245090202 | FDA UDI | Class II | Unknown |
| Up & Up | 245-07-1174 | FDA UDI | Class I | Active |
| up & up | 094 01 0632 (67856TG3) | FDA UDI | Class I | Active |
| Up&Up | 094010238 | FDA UDI | Class I | Unknown |
| Up & Up | Digital Pregnancy Test | FDA UDI | Class II | Unknown |
| Up & Up | DT002 | FDA UDI | Class II | Active |
| Up&Up | 245-03-0094 | FDA UDI | Class II | Unknown |
| Up & Up | Early Result Pregnancy Test | FDA UDI | Class II | Unknown |
| Up & Up | 245-07-0293 | FDA UDI | Class I | Active |
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