Invuity, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Invuity, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 4 cleared submissions from 2009 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Invuity, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Invuity, Inc.
4 devices
Cleared
Mar 06, 2020
PhotonBlade with Smoke Evacuation
General & Plastic Surgery
266d
Cleared
Sep 15, 2016
PhotonBlade
General & Plastic Surgery
52d
Cleared
Feb 10, 2012
EIGR SURGICAL ILLUMINATION SYSTEM
General & Plastic Surgery
56d
Cleared
Apr 22, 2009
INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM
General & Plastic Surgery
100d