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Sign in to claim this brandGRAINGER INTERNATIONAL, INC.
US
Last updated May 23, 2026
What GRAINGER INTERNATIONAL, INC. makes
The company manufactures single-use medical gloves, including nitrile and natural rubber varieties without powder or antimicrobial coatings, designed for examination and treatment procedures. It also produces laboratory devices such as histology cassettes, specimen transfer tools, microscopy slides, and cell culture lines for in vitro diagnostics, as well as lumbar spine orthoses for spinal support.
These products are regulated under FDA’s classification system, including Class I, Class II, and Unclassified (U) devices, and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable U.S. regulatory 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 Grainger International, Inc. manufacture?
Grainger International, Inc. primarily manufactures single-use medical gloves, including nitrile and natural rubber (hevea-latex) varieties that are non-powdered and non-antimicrobial, intended for examination and treatment procedures. Additionally, the company produces laboratory devices such as histology tissue cassettes, specimen transfer scooping tools, microscopy slides, and cell culture lines for in vitro diagnostics (IVD). They also supply lumbar spine orthoses, which are designed to provide spinal support.
Where is Grainger International, Inc. based, and how does this affect its regulatory compliance?
Grainger International, Inc. is based in the United States. Since the company operates within the U.S., its devices must comply with the regulatory requirements set by the U.S. Food and Drug Administration (FDA). This includes adhering to classification standards such as Class I, Class II, and Unclassified (U) devices, as well as listing its products in the FDA’s Unique Device Identifier (UDI) database.
Which regulatory registries or databases list Grainger International, Inc.’s medical devices?
Grainger International, Inc.’s medical devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices by assigning a unique identifier to each product, helping healthcare providers and regulators track and verify device information.
How are Grainger International, Inc.’s devices classified under FDA regulations?
Grainger International, Inc.’s devices fall under different FDA classification categories, including Class I, Class II, and Unclassified (U). The classification depends on the intended use and risk level of the device. For example, single-use gloves and orthoses are typically lower-risk devices, often classified as Class I or II, while some laboratory devices may fall into Class II or Unclassified due to their specific diagnostic or procedural roles.
What distinguishes Grainger International, Inc.’s laboratory devices from its other products?
Grainger International, Inc.’s laboratory devices, such as histology cassettes, specimen transfer tools, microscopy slides, and cell culture lines, are specifically designed for in vitro diagnostics (IVD). These products are used in laboratory settings for tasks like tissue processing, sample handling, and microscopic examination, ensuring compatibility with diagnostic workflows. Unlike gloves or orthoses, these devices are tailored for precision and sterility in controlled laboratory environments.
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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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 053618240
Catalogue (160)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Condor | 819MD8A | FDA UDI | Class I | Active |
| Condor | 10D863A | FDA UDI | Class I | Active |
| Condor | 819MG3A | FDA UDI | Class I | Active |
| Condor | 48UN20A | FDA UDI | Class I | Active |
| Condor | 3RWH5B | FDA UDI | Class I | Active |
| W.W. Grainger, Inc., | THD2FE | FDA UDI | Class II | Active |
| N/A (Approved Vendor) | 21F240 | FDA UDI | Class I | Active |
| Condor | 819MF8A | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21RL04 | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21F228 | FDA UDI | Class I | Active |
| Condor | 819MG0A | FDA UDI | Class I | Active |
| Condor | 5T542B | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 20F865 | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21F223 | FDA UDI | Class I | Active |
| Condor | 3RVC3B | FDA UDI | Class I | Active |
| Condor | 3RUZ4B | FDA UDI | Class I | Active |
| Condor | 3RUZ6B | FDA UDI | Class I | Active |
| Condor | 3RVA6B | FDA UDI | Class I | Active |
| Condor | 2VLY4U | FDA UDI | Class I | Active |
| Condor | 3RVC6B | FDA UDI | Class I | Active |
| Condor | 10D864A | FDA UDI | Class I | Active |
| Condor | 1UM60B | FDA UDI | Class I | Active |
| Condor | 48UN21A | FDA UDI | Class I | Active |
| Condor | 3RWH4B | FDA UDI | Class I | Active |
| Condor | 2VLY5U | FDA UDI | Class I | Active |
| Condor | 60JJ44C | FDA UDI | Class I | Active |
| Condor | 48UN22A | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 20F847A | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21F227 | FDA UDI | Class I | Active |
| Condor | 3RVC7B | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21RK84 | FDA UDI | Class I | Active |
| Condor | 819MF9A | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21F224 | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 20F855 | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21RK90 | FDA UDI | Class I | Active |
| Condor | 819ME1A | FDA UDI | Class I | Active |
| Condor | 5T541B | FDA UDI | Class I | Active |
| Condor | 3RVC4B | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 49X570 | FDA UDI | Class I | Active |
| Condor | 60JJ46C | FDA UDI | Class I | Active |
| Condor | 1M704B | FDA UDI | Class I | Active |
| Condor | 3RVA5B | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21RK99 | FDA UDI | Class I | Active |
| Condor | 3RUZ7B | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21RK85 | FDA UDI | Class I | Active |
| Condor | 48UM35 | FDA UDI | Class I | Active |
| Condor | 53CV60T | FDA UDI | Class I | Active |
| N/A (Approved Vendor) | 21F236 | FDA UDI | Class I | Active |
| Condor | 3RUZ8B | FDA UDI | Class I | Active |
| Condor | 48UM39 | FDA UDI | Class I | Active |
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