Vector R&D, Inc.
Country not established
Vector R&D, Inc. is a medical device manufacturer, with 118 devices listed in FDA GUDID (FDA Class I and II) as of 12 Nov 2026.
- Devices
- 118
Registry facts
- Registries
- FDA GUDID 118
- Device classes
- FDA Class I 114
- FDA Class II 4
- Identifiers
- DUNS 825399723
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.
Catalogue
Search and filter all 118 devicesShowing 1-50 of 118
Company details
- DUNS number
- 825399723
- mattr@vectorusa.net
- Phone
- +1(253)263-7208
Frequently asked questions
How many devices does Vector R&D, Inc. have in the registry?
The registry currently lists 118 devices for Vector R&D, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vector R&D, Inc.'s devices?
Among its 50 most recently registered devices, Vector R&D, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Vector R&D, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Vector R&D, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vector R&D, Inc. in the registry?
The most recently registered devices listed for Vector R&D, Inc. include Vector R&D, Inc DRA-NK, Vector R&D, Inc F4, Vector R&D, Inc VM25LPA and Vector R&D, Inc KV80.