# Intersect Ent.

- Location (FDA's records): Menlo Park
- FDA decisions: 2 (2011–2022): 1 510(k) clearance and 1 original PMA approval
- Product codes: OWO (1), LRC (1)
- Predicates its devices cite: 1 (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
- Entellus Medical, Inc.: 1 (https://510kreport.com/company/entellus-medical)

## Firms that cite its devices most
- Fiagon GmbH: 1 (https://510kreport.com/company/fiagon)

## Its most-cited devices
- K212774: VenSure LightGuide (2022), cited by 1

## Recent decisions
- K212774: VenSure LightGuide (Feb 4, 2022)
- P100044: Propel (Aug 11, 2011)

Source page: https://510kreport.com/company/intersect-ent