Universal Implant Systems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Universal Implant Systems, Inc. makes
Universal Implant Systems, Inc. manufactures dental implant products, including the UNIPLANT Dental Implant System and the OCTA-HEX™ Implant Restoration Systems, which are used for tooth replacement and restoration procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Uniplant Dental Implant System Ref K011574
510(k) 510(k)Octa-Hex (Tm) Implant Restoration Systems Ref K905223
510(k) 510(k)
Frequently asked questions
How many devices does Universal Implant Systems, Inc. have in the registry?
The registry currently lists 2 devices for Universal Implant Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Universal Implant Systems, Inc.'s devices?
Among its 2 most recently registered devices, Universal Implant Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Universal Implant Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Universal Implant Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Universal Implant Systems, Inc. in the registry?
The most recently registered devices listed for Universal Implant Systems, Inc. include UNIPLANT DENTAL IMPLANT SYSTEM and OCTA-HEX (TM) IMPLANT RESTORATION SYSTEMS.