# Pontis Orthopaedics, LLC

- Location (FDA's records): San Francisco, CA
- FDA decisions: 2 (2014–2014): 2 510(k) clearances
- Product codes: GAQ (1), MBI (1)
- Predicates its devices cite: 7 (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
- Core Essence Orthopaedics, LLC: 3 (https://510kreport.com/company/core-essence-orthopaedics)
- Depuy Mitek, A Johnson & Johnson Company: 1 (https://510kreport.com/company/depuy-mitek-a-johnson-johnson)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Smith & Nephew Inc., Endoscopy Division: 1 (https://510kreport.com/company/smith-nephew-endoscopy-division)
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)

## Firms that cite its devices most
- Resorba Medical GmbH: 1 (https://510kreport.com/company/resorba-medical)

## Its most-cited devices
- K140127: Ferrofibre Stainless Steel Suture with Crimp (2014), cited by 1

## Recent decisions
- K133579: Multifilament Stainless Steel Sutures with Crimps (Jun 26, 2014)
- K140127: Ferrofibre Stainless Steel Suture with Crimp (May 28, 2014)

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