# Bionime Coporation

- Location (FDA's records): San Juan Capistrano, CA
- FDA decisions: 3 (2014–2015): 3 510(k) clearances
- Product codes: NBW (3)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 2 (0 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
- Bionime Corporation: 9 (https://510kreport.com/company/bionime)

## Firms that cite its devices most
- Bionime Corporation: 2 (https://510kreport.com/company/bionime)

## Its most-cited devices
- K143387: GE333 Blood Glucose Monitoring System (2015), cited by 2

## Recent decisions
- K141292: Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose Monitoring System GM650, GE200 Blood Glucose Monitoring System, and GE300 Talking Blood Glucose Monitoring System (Jun 9, 2015)
- K143387: GE333 Blood Glucose Monitoring System (Jun 3, 2015)
- K133522: Rightest Diabetes Management Software and Adapter (Existing Cleared K113007),Rightest New Adapters-3,GE Diabetes Managem (Apr 17, 2014)

Source page: https://510kreport.com/company/bionime-coporation