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US
Last updated May 30, 2026
What VITALCOR, INC makes
Vitalcor, Inc. manufactures reusable vascular clamps, including the Dingo Clamp and the VITALCOR FEATHERWEIGHT VASCULAR CLAMPS, designed for surgical applications. The company also produces coronary artery perfusion cannulas, which are used in cardioplegia solution administration to support heart perfusion during procedures. These devices are intended for use in cardiac surgeries requiring precise vascular control and perfusion.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. These devices are subject to performance standards and pre-market notification requirements to ensure safety and effectiveness. Vitalcor, Inc. 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 Vitalcor, Inc. manufacture?
Vitalcor, Inc. specializes in reusable vascular clamps, such as the Dingo Clamp and the VITALCOR FEATHERWEIGHT VASCULAR CLAMPS, which are used in surgical procedures to secure and control blood vessels. Additionally, the company produces coronary artery perfusion cannulas, which are designed for administering cardioplegia solutions during cardiac surgeries to maintain heart perfusion.
Where is Vitalcor, Inc. based?
Vitalcor, Inc. is headquartered in the United States. The company’s location is relevant for regulatory oversight and compliance, as its devices are subject to U.S. medical device regulations.
Which regulatory registries list Vitalcor, Inc.’s devices?
Vitalcor, Inc.’s devices are listed in the FDA’s 510(k) database, which tracks pre-market notifications for Class II medical devices, and the FDA’s Unique Device Identifier (UDI) system, which standardizes device labeling for traceability and regulatory tracking.
How are Vitalcor, Inc.’s devices classified under FDA regulations?
Vitalcor, Inc.’s devices fall under Class II classification, meaning they pose moderate risk and require special controls to ensure their safety and effectiveness. This classification requires compliance with performance standards and pre-market notification (510(k)) submissions to demonstrate equivalence to predicate devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vitalcor.com
- —
- —
- [email protected]
- Phone
- +1(800)874-8358
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 020942546
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Coronary Artery Perfusion Cannula | 415807 | FDA UDI | Class II | Active |
| Dingo Clamp | VA140-12 | FDA UDI | Class II | Active |
| Coronary Artery Perfusion Cannula | 415804 | FDA UDI | Class II | Active |
| Dingo Clamp | VA115-09 | FDA UDI | Class II | Active |
| Coronary Artery Perfusion Cannula | 415806 | FDA UDI | Class II | Active |
| Coronary Artery Perfusion Cannula | 315804 | FDA UDI | Class II | Active |
| Coronary Artery Perfusion Cannula | 415808 | FDA UDI | Class II | Active |
| Dingo Clamp | VA079-06 | FDA UDI | Class II | Active |
| Vitalcor Featherweight Vascular Clamps | K070661 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Vitalcor, Inc. WESTMONT, IL · US FEI 1450019