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Sign in to claim this brandInternational Marketing Specialists, Inc.
US
Last updated May 23, 2026
What International Marketing Specialists, Inc. makes
International Marketing Specialists, Inc. manufactures sharps disposal containers, including single-use Tiger Sharps Containers and reusable Tiger Reusable Sharps Containers designed for safe handling of used needles and sharp medical waste.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from 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 International Marketing Specialists, Inc. manufacture?
International Marketing Specialists, Inc. specializes in sharps disposal containers. Their product line includes single-use Tiger Sharps Containers and reusable Tiger Reusable Sharps Containers, both designed specifically for safely disposing of used needles and other sharp medical waste. These devices help reduce the risk of needle-stick injuries and improve waste management in healthcare settings.
Where is International Marketing Specialists, Inc. based?
The company is headquartered in the United States. This location allows them to operate within the regulatory framework of the FDA, which governs the classification and listing of their medical devices.
How are the devices manufactured by International Marketing Specialists, Inc. classified by regulatory authorities?
The devices produced by International Marketing Specialists, Inc., such as the Tiger Sharps Containers, are classified as Class II under FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, beyond general controls.
Which regulatory registries or databases list the devices made by International Marketing Specialists, Inc.?
The devices manufactured by International Marketing Specialists, Inc. are listed in the FDA’s 510(k) registry. The 510(k) pathway is used to demonstrate that a new device is substantially equivalent to a legally marketed predicate device, ensuring compliance with FDA requirements before commercial distribution.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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- DUNS Number
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Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tiger Sharps | MD008 | FDA UDI | Class II | Active |
| Tiger Sharps | MD001 | FDA UDI | Class II | Active |
| Tiger Sharps | RMD002B | FDA UDI | Class II | Active |
| Tiger Sharps | RMD003A | FDA UDI | Class II | Active |
| Tiger Sharps | RMD002A | FDA UDI | Class II | Active |
| Tiger Sharps | RMD003B | FDA UDI | Class II | Active |
| Tiger Sharps | MD005 | FDA UDI | Class II | Active |
| Tiger Sharps | MD002 | FDA UDI | Class II | Active |
| Tiger Sharps Containers | K190240 | FDA 510(k) | Class II | Active |
| Tiger Reusable Sharps Container | K203305 | FDA 510(k) | Class II | Active |
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