# Invuity, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 4 (2009–2020): 4 510(k) clearances
- Product codes: FST (2), GEI (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Thompson Surgical Instruments, Inc.: 1 (https://510kreport.com/company/thompson-surgical-instruments)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Peak Surgical, Inc.: 1 (https://510kreport.com/company/peak-surgical)
- Coral Medical, Inc.: 1 (https://510kreport.com/company/coral-medical)

## Firms that cite its devices most
- Katalyst Surgical, LLC: 1 (https://510kreport.com/company/katalyst-surgical)

## Its most-cited devices
- K162053: PhotonBlade (2016), cited by 1
- K113697: Eigr Surgical Illumination System (2012), cited by 1

## Recent decisions
- K191583: PhotonBlade with Smoke Evacuation (Mar 6, 2020)
- K162053: PhotonBlade (Sep 15, 2016)
- K113697: Eigr Surgical Illumination System (Feb 10, 2012)
- K090070: Invuity Britefield Mcculloch Retractor System (Apr 22, 2009)

Source page: https://510kreport.com/company/invuity