Acell, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
FDA 510(k) cleared devices by Acell, Inc. General & Plastic Surgery ✕
19 devices
Cleared
Jul 11, 2024
MicroMatrix® UBM Particulate
General & Plastic Surgery
28d
Cleared
Jul 11, 2024
Cytal® Wound Matrix
General & Plastic Surgery
27d
Cleared
Sep 22, 2023
MicroMatrix® Flex
General & Plastic Surgery
170d
Cleared
Oct 25, 2019
Cytal Wound Matrix 3-Layer
General & Plastic Surgery
28d
Cleared
Feb 07, 2019
Gentrix Surgical Matrix, Gentrix Surgical Matrix Hiatal
General & Plastic Surgery
170d
Cleared
May 11, 2018
Cytal Wound Particulate
General & Plastic Surgery
49d
Cleared
Oct 06, 2017
MicroMatrix
General & Plastic Surgery
59d
Cleared
Jun 08, 2017
Gentrix Surgical Matrix Thick
General & Plastic Surgery
87d
Cleared
Oct 21, 2016
Gentrix Surgical Matrix
General & Plastic Surgery
38d
Cleared
Mar 14, 2016
MicroMatrix
General & Plastic Surgery
76d
Cleared
Dec 08, 2015
Cytal Wound Matrix
General & Plastic Surgery
78d
Cleared
Jun 17, 2015
Matristem Surgery Matrix RS, PSM, PSMX, Matristem Pelvic Floor Matrix
General & Plastic Surgery
415d
Cleared
Aug 29, 2011
MATRISTEM WOUND MATRIX
General & Plastic Surgery
7d
Cleared
Oct 28, 2009
ACELL MATRISTEM WOUND SHEET
General & Plastic Surgery
35d
Cleared
Jun 23, 2006
ACELL POWDER WOUND DRESSING
General & Plastic Surgery
84d
Cleared
Jul 07, 2004
ACELL UBM SURGICAL MESH ML AND MLPLUS
General & Plastic Surgery
68d
Cleared
Apr 14, 2004
ACELL UBM SURGICAL MESH
General & Plastic Surgery
36d
Cleared
Dec 30, 2002
ACELL UBM HYDRATED WOUND DRESSING
General & Plastic Surgery
137d
Cleared
Dec 19, 2002
ACELL UBM LYOPHILIZED WOUND DRESSING
General & Plastic Surgery
216d