# Conextions Medical

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 2 (2020–2022): 2 510(k) clearances
- Product codes: GAQ (1), MBI (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 1 (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
- Ortheon Medical, LLC: 1 (https://510kreport.com/company/ortheon-medical)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)
- Ziptek, LLC: 1 (https://510kreport.com/company/ziptek)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Firms that cite its devices most
- BAAT Medical Products B.V.: 1 (https://510kreport.com/company/baat-medical-products)

## Its most-cited devices
- K200028: Coronet Soft Tissue Fixation System (2020), cited by 1

## Recent decisions
- K203855: CoNextions TR Tendon Repair System (Apr 22, 2022)
- K200028: Coronet Soft Tissue Fixation System (Mar 4, 2020)

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