FDA 510(k) Applications Submitted by restor3d, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K240591 03/01/2024 restor3d Kinos Axiom Total Ankle System restor3d, Inc.
K242356 08/08/2024 TIDAL Fusion Cage System restor3d, Inc.
K243768 12/06/2024 iTotal« IdentityÖ Cruciate Retaining 3DP Porous Knee Replacement System restor3d, inc.
K201314 05/18/2020 Restor3d Utility Wedge restor3d, Inc.
K201393 05/27/2020 restor3d MTP Implant Restor3d, Inc.


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