# Ibalance Medical, Inc.

- Location (FDA's records): Philedelphia, PA
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: HRS (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (0 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
- Cayenne Medical, Inc.: 2 (https://510kreport.com/company/cayenne-medical)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Spine Wave, Inc.: 1 (https://510kreport.com/company/spine-wave)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Recent decisions
- K092381: Ibalance Akrfx Medial Opening Wedge Tibial System, Ifx Medial Peek Implant and Anchor, Akrfx Instrumentation (Oct 27, 2009)

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