# Mckenna & Cuneo

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (1995–1997): 3 510(k) clearances
- Product codes: GWF (1), LKY (1), LYG (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Encore, Inc.: 1 (https://510kreport.com/company/encore)
- Neurometrix, Inc.: 1 (https://510kreport.com/company/neurometrix)
- Tonica Elektronik A/S: 1 (https://510kreport.com/company/tonica-elektronik-a-s)
- Medtronic Functional Diagnostics A/S: 1 (https://510kreport.com/company/medtronic-functional-diagnostics-a-s)
- Laborie Medical Technologies, Ltd.: 1 (https://510kreport.com/company/laborie-medical-technologies)

## Its most-cited devices
- K944547: Dantec Keypoint (1995), cited by 4
- K971257: Vtu-1 Vacuum Erection System (1997), cited by 1

## Recent decisions
- K971257: Vtu-1 Vacuum Erection System (Oct 3, 1997)
- K936312: Manual Massage Roller (Jan 29, 1996)
- K944547: Dantec Keypoint (Sep 19, 1995)

Source page: https://510kreport.com/company/mckenna-cuneo