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Lsi Solutions, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
DEN230069Mi-CHORD SystemJune 11, 2024
K222783MD Mattress Suture Placement DeviceJanuary 12, 2024
K202551Cor-Knot MicroJune 24, 2021
K203120RD QUICK LOAD SUTURE, 0 Polyester, RD QUICK LOAD SUTURE, 2-0 Polyester, RD QUCIK LOAD SUTURE, 2-0 PoNovember 24, 2020
K203081RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical SutureNovember 24, 2020
K163639LS-5 ePTFE SutureJune 2, 2017
K111014LSI SOLUTIONS FORNISEE SYSTEM UTERINE MANIPULATOR AND ACCESSORIESJuly 13, 2012
K100593SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SEROctober 13, 2010
K040232LSI SEW-RIGHT R SERIES SUTURE PLACEMENT DEVICE AND ACCESS PRODUCT SEW-RIGHT SR-5R, MODEL 020999March 1, 2004
K031443LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTSJune 18, 2003
K024301LSI ENDOSCOPIC EXTERNAL ACCESSORY CHANNEL AND ACCESSORIES PRODUCTMarch 24, 2003
K011016LSI SOLUTIONS FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES PRODUCTApril 27, 2001
K981531SUTURE PLACEMENT DEVICE AND ACCESSORIESJuly 13, 1998
K963919LSI VIDEOSCOPIC DISPLAY SYSTEMJanuary 8, 1997