# K012753: Soring GMBH Sonoca 180/190

- Pathway: 510(k) (Traditional)
- Applicant: Soring GmbH Medizintechnik
- Decided: Nov 13, 2001 after 89 days
- Product code: LFL (Instrument, Ultrasonic Surgical)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K942095 (1994). 2 ancestors in all.
6 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992026: Soring GMBH, Sonoca 300, Soring GmbH Medizintechnik (1999) Summary page 1.

## Most influential descendants
- K062544: AR1000 Ultrasonic Wound Therapy System (2007), 5 descendants of its own
- K112782: Misonix Sonicone (R) Ultrasonic Wound Care System and Accessories (2011), 2 descendants of its own
- K072904: Sonoca 180/195 Wound Care System (2008), 1 descendant of its own
- K131096: AR1000 Series Ultrasonic Wound Therapy System (2014), 0 descendants of its own
- K123980: Sonicone Plus Ultrasound Wound Care System and Accessories (2013), 0 descendants of its own

## Indications for use
The SONOCA 180/190 is an instrument intended for selected ultrasound dissection and fragmenting of tissue at the operation site during multi-medical discipline surgery including: General Surgery, Neuro, Thoracic, Urology, and Gastro-intestinal modalities. Typical users of this system are trained professionals; physicians, nurses, and technicians.

Source page: https://510kreport.com/device/K012753
Methodology: https://510kreport.com/methodology