# Vibronics

- Location (FDA's records): Danville, CA
- FDA decisions: 1 (1991–1991): 1 510(k) clearance
- Product codes: KNW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medical Device Technologies, Inc.: 1 (https://510kreport.com/company/medical-device-technologies)
- Promex Technologies, LLC: 1 (https://510kreport.com/company/promex-technologies)
- Inrad: 1 (https://510kreport.com/company/inrad)

## Its most-cited devices
- K904987: Vibronics Auto Core Biopsy Device (Acbd) (1991), cited by 3

## Recent decisions
- K904987: Vibronics Auto Core Biopsy Device (Acbd) (Feb 11, 1991)

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