# Acueity, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 4 (2001–2004): 4 510(k) clearances
- Product codes: KNW (1), GCT (1), FCW (1), GCJ (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Promex, Inc.: 1 (https://510kreport.com/company/promex)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Dofi Technologies, Inc.: 1 (https://510kreport.com/company/dofi-technologies)
- Welch Allyn, Inc.: 1 (https://510kreport.com/company/welch-allyn)

## Firms that cite its devices most
- C-Link Micro Imaging, Inc.: 1 (https://510kreport.com/company/c-link-micro-imaging)
- Davlite Technologies: 1 (https://510kreport.com/company/davlite-technologies)
- Acclarent, Inc.: 1 (https://510kreport.com/company/acclarent)
- Millennium Devices, Inc.: 1 (https://510kreport.com/company/millennium-devices)
- Cytyc Surgical Products: 1 (https://510kreport.com/company/cytyc-surgical-products)

## Its most-cited devices
- K011189: Viaduct Microendoscope and Accessories (2001), cited by 6

## Recent decisions
- K040949: Viaduct Miniscope and Accessories (May 7, 2004)
- K032847: Excisor Bioptome, Model 01-0004 (Sep 26, 2003)
- K032430: Acueity Medical Light Source (Sep 5, 2003)
- K011189: Viaduct Microendoscope and Accessories (Jul 16, 2001)

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