# Pontis Orthopaeeics, LLC

- Location (FDA's records): San Francisco, CA
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: MBI (1)
- Predicates its devices cite: 1 (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
- Core Essence Orthopaedics, LLC: 1 (https://510kreport.com/company/core-essence-orthopaedics)

## Recent decisions
- K141711: Pontis 3MM Suture Anchors with Ultra-High Molecular Weight Polyethylene Suture, Pontis Ultra-High Molecular Weight Polye (Jul 24, 2014)

Source page: https://510kreport.com/company/pontis-orthopaeeics