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Sign in to claim this brandOp-Co Medical Products , Ltd.
US
Last updated May 23, 2026
What Op-Co Medical Products , Ltd. makes
Op-Co Medical Products, Ltd. manufactures medical devices for secure intravenous (IV) administration, including the SECURE-SITE for puncture-resistant port protection and the SECURODRIP I.V. ARMBOARD, a stabilizing armboard for IV lines. The SECURODRIP is designed as a standalone IV administration set with integrated safety features.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) registry. 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 Op-Co Medical Products, Ltd. manufacture?
Op-Co Medical Products, Ltd. specializes in medical devices designed for secure intravenous (IV) administration. Their portfolio includes puncture-resistant port protection devices like the SECURE-SITE and IV administration systems like the SECURODRIP, which is also available as the SECURODRIP I.V. ARMBOARD. These products focus on enhancing safety and stability during IV therapy by incorporating features like puncture resistance and arm stabilization.
Where is Op-Co Medical Products, Ltd. based?
Op-Co Medical Products, Ltd. is headquartered in the United States. The company’s location in the US aligns with its regulatory focus on FDA compliance, as evidenced by its devices being listed in the FDA’s 510(k) registry.
Which regulatory registries list Op-Co Medical Products, Ltd.’s devices?
Op-Co Medical Products, Ltd.’s devices are included in the FDA’s 510(k) registry. This registry tracks medical devices that have undergone a 510(k) premarket notification process, demonstrating that the company’s products meet FDA requirements for safety and effectiveness as Class I devices.
How are Op-Co Medical Products, Ltd.’s devices classified under FDA regulations?
Op-Co Medical Products, Ltd.’s devices are classified as Class I under FDA regulations. Class I devices are generally considered to pose the lowest risk and often require less regulatory oversight, though they still must comply with FDA requirements to ensure safety and proper performance.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Promedical Surgical Drapes, Promedical Surgical Mayo Stand Cover, Band Bags | K080629 | FDA 510(k) | Class II | Active |
| Promedical Surgical Mayo Stand Covers, Band Bags, Table Covers And Equipment Covers | K042137 | FDA 510(k) | Class II | Active |
| Secure-Site | K941098 | FDA 510(k) | Class I | Active |
| Promedical Surgical Drapes | K042131 | FDA 510(k) | Class II | Active |
| Promedical Surgical Gown, Models 18-301, 18-401 And 18-501 | K091097 | FDA 510(k) | Class II | Active |
| Promedical Surgical Gowns | K042111 | FDA 510(k) | Class II | Active |
| BH Sterilization Pouch | K172280 | FDA 510(k) | Class II | Active |
| 3l Surgical Drapes | K043015 | FDA 510(k) | Class II | Active |
| SURGICAL FACE MASK (Ear Loops and Tie-on) | K133070 | FDA 510(k) | Class II | Active |
| Securodrip | K912660 | FDA 510(k) | Class I | Active |
| Promedical Surgical Gowns, Models: 1002494a, 100770a | K080627 | FDA 510(k) | Class II | Active |
| BH Medical Dental Barrier Sleeves and Barrier Film | K190484 | FDA 510(k) | Class II | Active |
| Securodrip (tm) I.v. Armboard | K932757 | FDA 510(k) | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- BH Medical Products Co., Ltd Changzhou City Jiangsu · CN FEI 3009307523