# Infront Medical, LLC

- Location (FDA's records): Clifton, NJ
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 2 (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
- Synthes Spine: 2 (https://510kreport.com/company/synthes-spine)
- Stryker Spine: 2 (https://510kreport.com/company/stryker-spine)
- Sapphire Medical Group: 1 (https://510kreport.com/company/sapphire-medical-group)
- Vertebron, Inc.: 1 (https://510kreport.com/company/vertebron)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)

## Firms that cite its devices most
- Rubicon Spine, LLC: 1 (https://510kreport.com/company/rubicon-spine)
- Bethesda Medical Devices: 1 (https://510kreport.com/company/bethesda-medical-devices)

## Its most-cited devices
- K141443: Infront Lumbar Interbody Fusion System (2014), cited by 2

## Recent decisions
- K141443: Infront Lumbar Interbody Fusion System (Aug 28, 2014)

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