Is this your brand? Sign in to claim ownership.
Sign in to claim this brandHealthcare Products Plus, Inc.
US
Last updated May 23, 2026
What Healthcare Products Plus, Inc. makes
Healthcare Products Plus, Inc. manufactures the Needlyzer Needle Destroyer Model ND2, a device designed for the safe disposal of used needles to prevent sharps injuries and contamination.
The Needle Destroyer Model ND2 is classified as a Class II medical device and is listed under the FDA’s Premarket Approval (PMA) pathway. The company is based 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 Healthcare Products Plus, Inc. manufacture?
Healthcare Products Plus, Inc. specializes in devices focused on safety and infection control. Their primary product is the Needlyzer Needle Destroyer Model ND2, which is designed specifically for the safe disposal of used needles. This device helps healthcare settings reduce the risk of sharps injuries and contamination by mechanically destroying needles after use.
Where is Healthcare Products Plus, Inc. based, and how does that affect their regulatory oversight?
Healthcare Products Plus, Inc. is based in the United States. Since the company operates within the U.S., its devices are subject to regulatory oversight by the FDA, which aligns with the country’s medical device regulations. This means compliance with U.S. standards and reporting requirements applies to their products, including the Needlyzer Needle Destroyer Model ND2.
How are the devices manufactured by Healthcare Products Plus, Inc. classified under FDA regulations?
The Needlyzer Needle Destroyer Model ND2, produced by Healthcare Products Plus, Inc., is classified as a Class II medical device by the FDA. Class II devices generally pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. This classification influences the regulatory pathway, such as Premarket Approval (PMA), which applies to this specific device.
Which regulatory registries or databases list the devices made by Healthcare Products Plus, Inc.?
The Needlyzer Needle Destroyer Model ND2 is listed under the FDA’s Premarket Approval (PMA) pathway. This means the device’s details, including its regulatory status and compliance information, are documented in the FDA’s official records. While the company itself isn’t listed in a broader registry, individual devices like this one are tracked through the FDA’s approval processes and databases.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Koko Peak Kp; Koko Peak Kp+ | K010009 | FDA 510(k) | Class II | Active |
| Kp + Lfm | K013489 | FDA 510(k) | Class II | Active |
| The Needlyzer - The Needle Destroyer Model Nd2 | P960018 | FDA PMA | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.