Incisive Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Incisive Surgical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Incisive Surgical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Minnetonka, US.
Historical record: 5 cleared submissions from 2003 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Incisive Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Incisive Surgical, Inc.
5 devices
Cleared
Mar 16, 2012
INSORB ABSORBALBE STAPLE
General & Plastic Surgery
39d
Cleared
Feb 06, 2009
INSORB ABSORBABLE STAPLE, MODEL 1020, 1025, AND OTHER PRODUCT FAMILIES
General & Plastic Surgery
15d
Cleared
Jul 26, 2006
INSORB ABSORBABLE STAPLE, MODEL 1020
General & Plastic Surgery
30d
Cleared
Dec 16, 2003
INSORB ABSORBABLE STAPLE, MODEL SP-B20
General & Plastic Surgery
32d
Cleared
Apr 22, 2003
INSORB ABSORBABLE STAPLES, MODEL SP-B20
General & Plastic Surgery
130d