LK Consulting Group USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What LK Consulting Group USA, Inc. makes
LK Consulting Group USA, Inc. manufactures dental implant systems, including the JR Implant System, and intraoral imaging devices such as the EzDent-i, E2, and Prora View. The company also produces the KERATOR, a device used in dental diagnostics or treatment planning. These products are designed for use in oral and maxillofacial applications.
The company’s portfolio consists of Class II medical devices, all of which are listed via the FDA’s 510(k) pathway. These devices are regulated under U.S. jurisdiction and are intended for commercial distribution within the United States.
Catalogue
Jr Implant System Ref K130694
Regimes: 510(k) Registry: 510(k)EzDent-i /E2/Prora View Ref K150747
Regimes: 510(k) Registry: 510(k)Kerator Ref K132144
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does LK Consulting Group USA, Inc. have in the registry?
The registry currently lists 3 devices for LK Consulting Group USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LK Consulting Group USA, Inc.'s devices?
Among its 3 most recently registered devices, LK Consulting Group USA, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do LK Consulting Group USA, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for LK Consulting Group USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LK Consulting Group USA, Inc. in the registry?
The most recently registered devices listed for LK Consulting Group USA, Inc. include JR IMPLANT SYSTEM, EzDent-i /E2/Prora View and KERATOR.