# Sonokinetics, Inc.

- Location (FDA's records): Hoboken, NJ
- FDA decisions: 3 (1991–1999): 3 510(k) clearances
- Product codes: LFL (1), LZV (1), JDX (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 3 (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
- Valleylab, Inc.: 4 (https://510kreport.com/company/valleylab)
- Cooper Lasersonics, Inc.: 2 (https://510kreport.com/company/cooper-lasersonics)

## Firms that cite its devices most
- Omnisonics Medical Technologies: 1 (https://510kreport.com/company/omnisonics-medical-technologies)
- Penumbra, Inc.: 1 (https://510kreport.com/company/penumbra)

## Its most-cited devices
- K990572: Sonotome (1999), cited by 2
- K930629: Acryl-X II System (1994), cited by 1

## Recent decisions
- K990572: Sonotome (May 21, 1999)
- K930629: Acryl-X II System (Jan 21, 1994)
- K911548: Acryl-X System TM (Jun 28, 1991)

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