Entrigue Surgical, Inc. is one of 5205 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Entrigue Surgical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Entrigue Surgical, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 4 cleared submissions from 2007 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Entrigue Surgical, Inc. Filter by specialty or product code using the sidebar.
Entrigue Surgical, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
May 29, 2013
MEDIENT MIDDLE TURBINATE IMPLANT
Ear, Nose, Throat
106d
Cleared
Aug 29, 2012
SINUS DILATION SYSTEM
Ear, Nose, Throat
117d
Cleared
Jan 06, 2009
ENTACT SEPTAL STAPLER, MODEL 610-00100
Ear, Nose, Throat
109d
Cleared
Nov 16, 2007
BIOELAST 5-0 SUTURE, MODEL 500100
General & Plastic Surgery
73d