FDA 510(k) Applications for Medical Device Product Code "OXF"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K251224 | Acera Surgical, Inc. | Restrata Soft Tissue Reinforcement (STR) | 06/20/2025 |
| K123128 | ALLERGAN | SERI SURGICAL SCAFFOLD | 04/25/2013 |
| K243302 | PrintBio, Inc. | 3DMatrix DynaFlex (DynaFlex) | 05/21/2025 |
| K232602 | PrintBio, Inc. | 3DMatrix Surgical Mesh | 05/23/2024 |
| K172545 | Sofregen Medical, Inc. | SERI Contour | 09/22/2017 |
| K163217 | W. L. GORE & ASSOCIATES, INC. | GORE BIO-A Tissue Reinforcement | 02/10/2017 |
| K222919 | W. L. Gore and Associates, Inc. | GORE« ENFORM Biomaterial | 12/19/2022 |
| K173333 | W.L. Gore & Associates, Inc. | GORE ENFORM Biomaterial | 04/05/2018 |
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