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Sign in to claim this brandRamvac Dental Products, Inc.
US
Last updated May 31, 2026
What Ramvac Dental Products, Inc. makes
Ramvac Dental Products, Inc. manufactures dental suction systems designed for oral evacuation during dental procedures, including the RAMVAC series. These devices are engineered to manage saliva, water, and debris efficiently during treatments such as fillings, extractions, and cleanings.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. The devices are intended for use within the United States under applicable medical device regulations.
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 Ramvac Dental Products, Inc. manufacture?
Ramvac Dental Products, Inc. specializes in dental suction systems, such as the RAMVAC series. These devices are specifically designed for oral evacuation during dental procedures, helping to remove saliva, water, and debris during treatments like fillings, extractions, and cleanings. Their focus is on improving efficiency and comfort in dental care settings.
Where is Ramvac Dental Products, Inc. based?
Ramvac Dental Products, Inc. is based in the United States. The company’s operations and product development are aligned with U.S. medical device regulations, ensuring compliance with applicable standards for dental equipment.
Which regulatory registries list Ramvac Dental Products, Inc.’s devices?
Ramvac Dental Products, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their dental suction systems, including the RAMVAC series, under the U.S. regulatory framework.
How are Ramvac Dental Products, Inc.’s devices classified by regulatory authorities?
Ramvac Dental Products, Inc.’s dental suction systems fall under the FDA’s Class II regulatory classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 161936984
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