Velopex International, Inc.
Country not established FDA establishment FEI 3003697084
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Velopex International, Inc. makes
Velopex International, Inc. manufactures film processors for medical imaging, including the XTENDER Film Processor, Sprint Film Processor, and INTRAX Film Processor, as well as the Aquacut Fluid Abrasion Unit for dental applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Velopex Aquacut Fluid Abrasion Unit Ref K024105
510(k) 510(k)Intrax Film Processor Ref K093503
510(k) 510(k)
Company details
- FDA FEI number
- 3003697084
- Address
- 105 EAST 17TH ST., Saint Cloud, FL, 34769
Frequently asked questions
How many devices does VELOPEX INTERNATIONAL, INC. have in the registry?
The registry currently lists 3 devices for VELOPEX INTERNATIONAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VELOPEX INTERNATIONAL, INC.'s devices?
Among its 3 most recently registered devices, VELOPEX INTERNATIONAL, INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do VELOPEX INTERNATIONAL, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for VELOPEX INTERNATIONAL, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VELOPEX INTERNATIONAL, INC. in the registry?
The most recently registered devices listed for VELOPEX INTERNATIONAL, INC. include XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINT, VELOPEX AQUACUT FLUID ABRASION UNIT and INTRAX FILM PROCESSOR.