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Sign in to claim this brandVector R&D, Inc.
US
Last updated May 24, 2026
What Vector R&D, Inc. makes
Vector R&D, Inc. manufactures dental power tools, including motorless handpiece components, pneumatic and electric motorized handpieces, and pneumatic handpiece couplers. Their portfolio also includes pneumatic dental delivery systems designed for surgical and restorative procedures in dental settings.
The company’s devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer 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 Vector R&D, Inc. manufacture?
Vector R&D, Inc. specializes in dental power tools, including motorless handpiece components used in dental procedures, as well as pneumatic and electric motorized handpieces and sets. Their portfolio also covers pneumatic handpiece couplers and pneumatic dental delivery system instrument units, which are designed for both surgical and restorative dental applications.
Where is Vector R&D, Inc. based?
Vector R&D, Inc. is headquartered in the United States. This location is relevant for understanding the company’s regulatory framework, as it operates under U.S. medical device regulations.
Which regulatory registries list Vector R&D, Inc.’s devices?
Vector R&D, Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to identify and track specific devices.
How are Vector R&D, Inc.’s devices classified under FDA regulations?
Vector R&D, Inc.’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require less stringent regulatory controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway for each device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- vectorusa.net
- —
- —
- [email protected]
- Phone
- +1(253)263-7208
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 825399723
Catalogue (118)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vector R&D, Inc | TT-20K-OP | FDA UDI | Class I | Active |
| Vector R&D, Inc | F7-SLK | FDA UDI | Class I | Active |
| Vector R&D, Inc | CA-NK | FDA UDI | Class I | Active |
| Vector R&D, Inc | Vx9-SLK | FDA UDI | Class I | Active |
| Vector R&D, Inc | VNQD | FDA UDI | Class I | Active |
| Vector R&D, Inc | DRA-ST | FDA UDI | Class I | Active |
| Vector R&D, Inc | LMM-4 | FDA UDI | Class I | Active |
| Vector R&D, Inc | VSS5 | FDA UDI | Class I | Active |
| Vector R&D, Inc | VM10L-SG | FDA UDI | Class I | Active |
| Vector R&D, Inc | Vx10-SLN | FDA UDI | Class I | Active |
| Vector R&D, Inc | DPS-U | FDA UDI | Class I | Active |
| Vector R&D, Inc | AM1011 | FDA UDI | Class I | Active |
| Vector R&D, Inc | VM7P | FDA UDI | Class I | Active |
| Vector R&D, Inc | TT-LAP | FDA UDI | Class I | Active |
| Vector R&D, Inc | Vx9-SK | FDA UDI | Class I | Active |
| Vector R&D, Inc | CA-MW | FDA UDI | Class I | Active |
| Vector R&D, Inc | VWS4 | FDA UDI | Class I | Active |
| Vector R&D, Inc | TT-FPB-EC | FDA UDI | Class I | Active |
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