# K942095: Sonoca Iii

- Pathway: 510(k) (Traditional)
- Applicant: Holl Meditronics, Inc.
- Decided: Nov 9, 1994 after 203 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
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992026: Soring GMBH, Sonoca 300 (1999), 11 descendants of its own
- K012753: Soring GMBH Sonoca 180/190 (2001), 6 descendants of its own
- K062544: AR1000 Ultrasonic Wound Therapy System (2007), 5 descendants of its own
- K052183: Soring GMBH Sonoca Lipo (2005), 3 descendants of its own
- K112782: Misonix Sonicone (R) Ultrasonic Wound Care System and Accessories (2011), 2 descendants of its own

Source page: https://510kreport.com/device/K942095
Methodology: https://510kreport.com/methodology