Aziyo Biologics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aziyo Biologics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope (large), CanGaroo Envelope (extra large), CanGaroo Enevlope (extra extra large) (SubQ), CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope (large), CanGaroo Envelope (extra large), CanGaroo Envelope (extra extra large) (SubQ), CanGaroo Neuro Envelope (small)
4
Total
4
Cleared
0
Denied
Aziyo Biologics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Roswell, US.
Historical record: 4 cleared submissions from 2017 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aziyo Biologics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aziyo Biologics, Inc.
4 devices
Cleared
Jun 15, 2020
CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope...
General & Plastic Surgery
28d
Cleared
Oct 21, 2019
CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope...
General & Plastic Surgery
28d
Cleared
Nov 15, 2018
CanGaroo Neuro Envelope (small)
General & Plastic Surgery
87d
Cleared
Oct 25, 2017
CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope...
General & Plastic Surgery
19d