Invuity, Inc.
Invuity, Inc. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Invuity, Inc.
FDA recalls by Invuity, Inc.
- Z-2778-2017 — INVUITY(R) PhotonBlade(TM), REF PB1
- Z-0007-2013 — BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Invuity, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.