Medical Device Manufacturer · US , Washington , DC

Acell, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 2002

Recent clearances: MicroMatrix® UBM Particulate, Cytal® Wound Matrix, MicroMatrix® Flex

View 20 510(k) Devices ↓

20

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Acell, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Nov 22, 2019

MatriStem UBM Pericardial Patch

Cardiovascular · 147d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Apr 27, 2026