# Mortise Medical, LLC

- Location (FDA's records): Logan, UT
- FDA decisions: 2 (2017–2017): 2 510(k) clearances
- Product codes: MBI (1), HTN (1)
- Predicates its devices cite: 6 (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
- Smith & Nephew, Inc.: 2 (https://510kreport.com/company/smith-nephew)
- Smith & Nephew Inc., Endoscopy Div.: 1 (https://510kreport.com/company/smith-nephew-endoscopy-div)
- Mtp Solutions, LLC: 1 (https://510kreport.com/company/mtp-solutions)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Recent decisions
- K172620: SyndesMetrics Syndesmosis Repair System (Nov 8, 2017)
- K171964: LigaMetrics Suture Anchors (Sep 19, 2017)

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