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Sign in to claim this brandSurgi-Pak, Inc.
US
Last updated May 24, 2026
What Surgi-Pak, Inc. makes
Surgi-Pak, Inc. manufactures single-use surgical and medical supplies, including absorbent tip applicators, radiopaque woven sponges, non-latex pressure bandages, medical fibre padding, stockinette, gauze pads, tubular support bandages, and non-medicated surgical procedure kits.
All products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) database. 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 Surgi-Pak, Inc. manufacture?
Surgi-Pak, Inc. specializes in single-use surgical and medical supplies. Their product line includes general-purpose absorbent tip applicators/swabs, radiopaque woven surgical sponges, non-latex pressure bandages, medical fibre padding, stockinette, woven gauze pads (non-antimicrobial), tubular support bandages (non-latex), and non-medicated surgical procedure kits. These devices are designed for one-time clinical use to support wound care, surgical procedures, and patient hygiene.
Where is Surgi-Pak, Inc. based, and how does that affect its regulatory standing?
Surgi-Pak, Inc. is headquartered in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies all of Surgi-Pak’s products as Class I medical devices, which are generally considered to pose the lowest risk to patients. This classification means the devices are subject to general controls (e.g., manufacturing practices, labeling requirements) but typically do not require pre-market approval.
Are Surgi-Pak, Inc.’s devices listed in any regulatory registries, and why does this matter?
Yes, Surgi-Pak, Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry assigns a unique identifier to each device, improving traceability, reducing medical errors, and facilitating post-market surveillance. Listing in the UDI database ensures healthcare providers and regulators can quickly verify device details, such as manufacturer information, model specifications, and batch details, which supports patient safety and compliance.
How are Surgi-Pak, Inc.’s devices classified by the FDA, and what does that mean for their use?
The FDA categorizes all of Surgi-Pak, Inc.’s devices as Class I, the lowest risk classification for medical devices. This classification means the devices are subject to basic regulatory controls, such as good manufacturing practices (GMP) and proper labeling, but they do not require pre-market approval or rigorous clinical trials. Class I devices are typically considered safe and effective through established manufacturing standards and are commonly used in routine clinical settings, such as surgical sponges, bandages, and applicators.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- nhpsurgipak.com
- —
- —
- [email protected]
- Phone
- 6269683335
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 152736971
Catalogue (141)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| National Hospital Packaging | 14-004 | FDA UDI | Class I | Active |
| National Hospital Packaging | 21-003 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-105 | FDA UDI | Class I | Active |
| National Hospital Packaging | 24-094 | FDA UDI | Class I | Active |
| National Hospital Packaging | 31-014 | FDA UDI | Class I | Active |
| National Hospital Packaging | 32-001 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-002WO | FDA UDI | Class I | Active |
| National Hospital Packaging | 19-004 | FDA UDI | Class I | Active |
| National Hospital Packaging | 19-001 | FDA UDI | Class I | Active |
| National Hospital Packaging | 34-004 | FDA UDI | Class I | Active |
| National Hospital Packaging | 38-048 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-026S | FDA UDI | Class I | Active |
| National Hospital Packaging | 28-004 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-031 | FDA UDI | Class I | Active |
| National Hospital Packaging | 11-003 | FDA UDI | Class I | Active |
| National Hospital Packaging | 11-036 | FDA UDI | Class I | Active |
| National Hospital Packaging | 11-034 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-026 | FDA UDI | Class I | Active |
| National Hospital Packaging | 30-018 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-003DB | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-015 | FDA UDI | Class I | Active |
| National Hospital Packaging | 11-006 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-008WO | FDA UDI | Class I | Active |
| National Hospital Packaging | 8234 | FDA UDI | Class I | Active |
| National Hospital Packaging | 18-004 | FDA UDI | Class I | Active |
| National Hospital Packaging | 7765 | FDA UDI | Class I | Active |
| National Hospital Packaging | 7643 | FDA UDI | Class I | Active |
| National Hospital Packaging | 8244 | FDA UDI | Class I | Active |
| National Hospital Packaging | 7633 | FDA UDI | Class I | Active |
| National Hospital Packaging | 28-010HF | FDA UDI | Class I | Active |
| National Hospital Packaging | 11-033 | FDA UDI | Class I | Active |
| National Hospital Packaging | 32-003 | FDA UDI | Class I | Active |
| National Hospital Packaging | 28-012 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-009 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-007DB | FDA UDI | Class I | Active |
| National Hospital Packaging | 14-012 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-023 | FDA UDI | Class I | Active |
| National Hospital Packaging | 10-600 | FDA UDI | Class I | Active |
| National Hospital Packaging | 28-010 | FDA UDI | Class I | Active |
| National Hospital Packaging | 13-006WO | FDA UDI | Class I | Active |
| National Hospital Packaging | 28-007 | FDA UDI | Class I | Active |
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