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HARBOR SAFETY PRODUCTS INC

US

Last updated May 30, 2026

What HARBOR SAFETY PRODUCTS INC makes

Harbor Safety Products Inc manufactures sharps disposal containers designed for the secure containment of used needles, blades, and other hazardous medical waste. Their products are engineered to prevent accidental punctures and comply with occupational safety standards for healthcare and clinical settings.

The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer operates from the United States, adhering to applicable medical device regulations for sharps disposal solutions.

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 Harbor Safety Products Inc manufacture?

Harbor Safety Products Inc specializes in sharps disposal containers, which are designed to securely hold used needles, blades, and other hazardous medical waste. These devices are engineered to minimize the risk of accidental punctures and comply with occupational safety standards for healthcare and clinical environments.

Where is Harbor Safety Products Inc based, and how does this affect its devices?

Harbor Safety Products Inc is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations, including classification under the FDA’s device classification system and mandatory listing in the FDA’s Unique Device Identification (UDI) system.

Which regulatory registries list Harbor Safety Products Inc’s devices?

Harbor Safety Products Inc’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and track specific devices.

How are Harbor Safety Products Inc’s devices classified by regulatory authorities?

Harbor Safety Products Inc’s sharps disposal containers fall under FDA Class II device classification. This classification is assigned based on the device’s intended use and risk level, requiring manufacturers to demonstrate compliance with specific performance standards and regulatory controls.

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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LinkedIn
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Facebook
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Email
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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
129731373

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Sharp Trap ST100
FDA UDI
Class IIActive

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