# Stabiliz Orthopaedics, Inc.

- Location (FDA's records): Exton, PA
- FDA decisions: 4 (2012–2026): 4 510(k) clearances
- Names in FDA's records: Stabiliz Orthopaedics, Inc. (2); Stabiliz Orthopaedics, LLC (2)
- Product codes: HRS (2), HWC (1), KTT (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 1 (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
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Zimmer, Inc.: 3 (https://510kreport.com/company/zimmer)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Its most-cited devices
- K120651: Stabiliz Fixation System (2012), cited by 1

## Recent decisions
- K260112: QuikFix External Fixator: Knee-Spanning Pack (Mar 23, 2026)
- K230053: SimpliFix Hip System (Apr 19, 2023)
- K130731: Stabiliz Fixation System - SPL Locking Screw (Jul 19, 2013)
- K120651: Stabiliz Fixation System (Nov 27, 2012)

Source page: https://510kreport.com/company/stabiliz-orthopaedics