Lsi Solutions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lsi Solutions - FDA 510(k) Cleared Devices
Recent clearances: RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical Suture
8
Total
8
Cleared
0
Denied
Lsi Solutions has 8 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 8 cleared submissions from 1997 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lsi Solutions Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lsi Solutions
8 devices
Cleared
Nov 24, 2020
RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical Suture
General & Plastic Surgery
42d
Cleared
Jun 02, 2017
LS-5 ePTFE Suture
General & Plastic Surgery
161d
Cleared
Mar 01, 2004
LSI SEW-RIGHT R SERIES SUTURE PLACEMENT DEVICE AND ACCESS PRODUCT SEW-RIGHT...
General & Plastic Surgery
28d
Cleared
Jun 18, 2003
LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS
General & Plastic Surgery
43d
Cleared
Mar 24, 2003
LSI ENDOSCOPIC EXTERNAL ACCESSORY CHANNEL AND ACCESSORIES PRODUCT
Gastroenterology & Urology
90d
Cleared
Apr 27, 2001
LSI SOLUTIONS FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES PRODUCT
General & Plastic Surgery
23d
Cleared
Jul 13, 1998
SUTURE PLACEMENT DEVICE AND ACCESSORIES
General & Plastic Surgery
75d
Cleared
Jan 08, 1997
LSI VIDEOSCOPIC DISPLAY SYSTEM
General & Plastic Surgery
100d