Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Acell, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories3
Latest FDA decision2024-07-11
TypeNumberDevice NameCodeDateActions
510(k) K241724 Cytal® Wound Matrix; Cytal® Burn MatrixKGN2024-07-11 View
510(k) K241706 MicroMatrix® UBM ParticulateKGN2024-07-11 View
510(k) K230980 MicroMatrix® FlexKGN2023-09-22 View
510(k) K191734 MatriStem UBM Pericardial PatchPSQ2019-11-22 View
510(k) K192725 Cytal Wound Matrix 3-LayerKGN2019-10-25 View
510(k) K182259 Gentrix Surgical Matrix, Gentrix Surgical Matrix HiatalFTM2019-02-07 View
510(k) K180776 Cytal Wound ParticulateKGN2018-05-11 View
510(k) K172399 MicroMatrixKGN2017-10-06 View
510(k) K170763 Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix ExtendFTM2017-06-08 View
510(k) K162554 Gentrix Surgical MatrixFTM2016-10-21 View
510(k) K153754 MicroMatrixKGN2016-03-14 View