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Sign in to claim this brandWILSON WOLF MANUFACTURING LLC
US
Last updated September 17, 2026
What WILSON WOLF MANUFACTURING LLC makes
Wilson Wolf Manufacturing LLC produces G-Rex blood/tissue storage and culture containers designed for laboratory use, supporting cell expansion and tissue engineering applications.
The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements.
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 Wilson Wolf Manufacturing LLC produce?
Wilson Wolf Manufacturing LLC specializes in blood and tissue storage and culture containers, specifically the G-Rex line. These devices are engineered for laboratory applications, particularly to support cell expansion and tissue engineering processes. The focus is on creating controlled environments for handling biological materials.
Where is Wilson Wolf Manufacturing LLC based?
Wilson Wolf Manufacturing LLC is based in the United States. The company’s location aligns with U.S. regulatory frameworks, which govern the design, manufacturing, and distribution of its medical devices.
Which regulatory registries or databases list Wilson Wolf Manufacturing LLC’s devices?
Wilson Wolf Manufacturing LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance with U.S. regulatory requirements for medical devices, particularly for Class I products like the G-Rex containers.
How are Wilson Wolf Manufacturing LLC’s devices classified under medical device regulations?
Wilson Wolf Manufacturing LLC’s devices, including the G-Rex blood/tissue storage and culture containers, are classified as Class I medical devices. This classification is based on their intended use in laboratory settings for cell expansion and tissue engineering, where they pose minimal risk to patients or users, requiring fewer regulatory controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 2100 Old Highway 8 NW, New Brighton, MN, 55112
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3004982543
- DUNS Number
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Catalogue (28)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| G-Rex | RU80550-TF | FDA UDI | Class I | Active |
| G-Rex | 80110-CS | FDA UDI | Class I | Active |
| G-Rex | 81100 | FDA UDI | Class I | Active |
| G-Rex | RU81100-CS | FDA UDI | Class I | Active |
| G-Rex | J81100-CS | FDA UDI | Class I | Active |
| G-Rex | G285500 | FDA UDI | Class I | Active |
| G-Rex | 80192M | FDA UDI | Class I | Active |
| G-Rex | RUO5500-CS | FDA UDI | Class I | Active |
| G-Rex | 81100-CS | FDA UDI | Class I | Active |
| G-Rex | 80300M | FDA UDI | Class I | Active |
| G-Rex | 80110S-CS | FDA UDI | Class I | Active |
| G-Rex | G285500-CS | FDA UDI | Class I | Active |
| G-Rex | RU81100 | FDA UDI | Class I | Active |
| G-Rex | 80055 | FDA UDI | Class I | Active |
| G-Rex | 80040S | FDA UDI | Class I | Active |
| G-Rex | RU80550-CS | FDA UDI | Class I | Active |
| G-Rex | G285500-RU | FDA UDI | Class I | Active |
| G-Rex | 80240M | FDA UDI | Class I | Active |
| G-Rex | G285500-TF | FDA UDI | Class I | Active |
| G-Rex | RU80550 | FDA UDI | Class I | Active |
| G-Rex | 85500S-CS | FDA UDI | Class I | Active |
| G-Rex | RU85500-TF | FDA UDI | Class I | Active |
| G-Rex | 80660M | FDA UDI | Class I | Active |
| G-Rex | 80120M | FDA UDI | Class I | Active |
| G-Rex | 80500 | FDA UDI | Class I | Active |
| G-Rex | 80110S | FDA UDI | Class I | Active |
| G-Rex | 80110 | FDA UDI | Class I | Active |
| G-Rex | RU80055 | FDA UDI | Class I | Active |
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