FDA 510(k) Applications Submitted by LK Consulting Group USA, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130694 | 03/14/2013 | JR IMPLANT SYSTEM | LK Consulting Group USA, Inc. |
| K150747 | 03/23/2015 | EzDent-i /E2/Prora View | LK Consulting Group USA, Inc. |
| K132144 | 07/11/2013 | KERATOR | LK Consulting Group USA, Inc. |
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