# Arobella Medical, LLC

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 3 (2007–2014): 3 510(k) clearances
- Product codes: NRB (2), LFL (1)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Celleration, Inc.: 3 (https://510kreport.com/company/celleration)
- Misonix, Inc.: 2 (https://510kreport.com/company/misonix)
- Smith & Nephew Wound Management: 2 (https://510kreport.com/company/smith-nephew-wound-management)
- Soering GmbH: 1 (https://510kreport.com/company/soering)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Soring GmbH Medizintechnik: 1 (https://510kreport.com/company/soring-medizintechnik)

## Firms that cite its devices most
- Misonix, Inc.: 1 (https://510kreport.com/company/misonix)
- Soering GmbH: 1 (https://510kreport.com/company/soering)

## Its most-cited devices
- K062544: AR1000 Ultrasonic Wound Therapy System (2007), cited by 4

## Recent decisions
- K131096: AR1000 Series Ultrasonic Wound Therapy System (May 16, 2014)
- K091038: AS 1000 Ultrasound Wound Therapy System (Jun 19, 2009)
- K062544: AR1000 Ultrasonic Wound Therapy System (Jan 3, 2007)

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