Entrigue Surgical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K130354 | MEDIENT MIDDLE TURBINATE IMPLANT; (SINGLE PACK-1 PAIR, FOUR PACK-4 PAIR) | May 29, 2013 |
| K121351 | SINUS DILATION SYSTEM | August 29, 2012 |
| K082750 | ENTACT SEPTAL STAPLER, MODEL 610-00100 | January 6, 2009 |
| K072470 | BIOELAST 5-0 SUTURE, MODEL 500100 | November 16, 2007 |