FDA 510(k) Applications Submitted by Kerecis Limited

FDA 510(k) Number Submission Date Device Name Applicant
K132343 07/30/2013 MARIGEN WOUND DRESSING KERECIS LIMITED
K190528 03/04/2019 MariGen Wound Extra Kerecis Limited
K202430 08/25/2020 Kerecis Reconstruct Kerecis Limited
K192612 09/20/2019 Kerecis Gingiva Graft Kerecis Limited
K213231 09/30/2021 Kerecis Silicone Kerecis Limited
K153364 11/20/2015 Kerecis SecureMesh Kerecis Limited


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