Prodrive Systems, Inc.
Country not established
- Devices
- 3
What Prodrive Systems, Inc. makes
Prodrive Systems, Inc. manufactures replacement turbine components for dental handpieces and a line of dental handpiece lubricants, including multi-purpose lubricants designed for maintenance and performance. Their products are intended for use in dental procedures to ensure proper function and hygiene of handpiece systems.
The company’s portfolio is classified under FDA’s Class I medical devices, with individual products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, and the company operates from the United States.
Catalogue
Prodrive Systems Replacement Turbine Ref K062219
Regimes: 510(k) Registry: 510(k)Prodrive Line Of Dental Handpieces Ref K090369
Regimes: 510(k) Registry: 510(k)Do-All Dental Handpiece Lubricant Ref K073353
Regimes: CE MDD 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prodrive Systems, Inc. have in the registry?
The registry currently lists 3 devices for Prodrive Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prodrive Systems, Inc.'s devices?
Among its 3 most recently registered devices, Prodrive Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Prodrive Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Prodrive Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Prodrive Systems, Inc. in the registry?
The most recently registered devices listed for Prodrive Systems, Inc. include PRODRIVE SYSTEMS REPLACEMENT TURBINE, PRODRIVE LINE OF DENTAL HANDPIECES and DO-ALL DENTAL HANDPIECE LUBRICANT.