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
K251844	06/16/2025	Kerecis SurgiBind (50241)	Kerecis Limited
K251845	06/16/2025	Marigen Wound Extra; Kerecis Silicone; Kerecis Parvus	Kerecis Limited
K243843	12/13/2024	Tendon Protect (50242)	Kerecis Limited
K241080	04/19/2024	Kerecis Parvus (50207)	Kerecis Limited