# Calibra Medical, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 3 (2010–2012): 3 510(k) clearances
- Product codes: OPP (3)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 6 (3 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
- Eli Lilly and Company: 1 (https://510kreport.com/company/eli-lilly)
- Biovalve Technologies, Inc.: 1 (https://510kreport.com/company/biovalve-technologies)

## Firms that cite its devices most
- Cequr SA: 2 (https://510kreport.com/company/cequr)
- Lifescan Europe, A Division of Cilag GmbH: 1 (https://510kreport.com/company/lifescan-europe-a-division-of-cilag)

## Its most-cited devices
- K093065: Finesse Personal Insulin Delivery Patch, Model FG-2000 (2010), cited by 3
- K100947: Finesse Personal Insulin Delivery Patch, Model FG 2000 (2010), cited by 2
- K111924: Finesse Personal Insulin Delivery Patch (2012), cited by 1

## Recent decisions
- K111924: Finesse Personal Insulin Delivery Patch (Apr 10, 2012)
- K100947: Finesse Personal Insulin Delivery Patch, Model FG 2000 (Jun 28, 2010)
- K093065: Finesse Personal Insulin Delivery Patch, Model FG-2000 (Jan 20, 2010)

Source page: https://510kreport.com/company/calibra-medical