# Entrigue Surgical, Inc.

- Location (FDA's records): San Antonio, TX
- FDA decisions: 4 (2007–2013): 4 510(k) clearances
- Product codes: LYA (1), NWJ (1), LRC (1), OLL (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 4 (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
- Walter Lorenz Surgical, Inc.: 1 (https://510kreport.com/company/walter-lorenz-surgical)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)
- Entellus Medical, Inc.: 1 (https://510kreport.com/company/entellus-medical)

## Firms that cite its devices most
- Spirair, Inc.: 1 (https://510kreport.com/company/spirair)
- Sinusys Corporation: 1 (https://510kreport.com/company/sinusys)
- Arthrocare Corp.: 1 (https://510kreport.com/company/arthrocare)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)

## Its most-cited devices
- K121351: Sinus Dilation System (2012), cited by 3
- K130354: Medient Middle Turbinate Implant; (Single Pack-1 Pair, Four Pack-4 Pair) (2013), cited by 1

## Recent decisions
- K130354: Medient Middle Turbinate Implant; (Single Pack-1 Pair, Four Pack-4 Pair) (May 29, 2013)
- K121351: Sinus Dilation System (Aug 29, 2012)
- K082750: Entact Septal Stapler, Model 610-00100 (Jan 6, 2009)
- K072470: Bioelast 5-0 Suture, Model 500100 (Nov 16, 2007)

Source page: https://510kreport.com/company/entrigue-surgical