Laurus Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laurus Medical Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Laurus Medical Corp. has 4 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 4 cleared submissions from 1994 to 1997. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Laurus Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laurus Medical Corp.
4 devices
Cleared
Dec 02, 1997
CURVILINEAR SUTURE PLACEMENT SYSTEM
General & Plastic Surgery
84d
Cleared
Nov 06, 1997
STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM
Gastroenterology & Urology
71d
Cleared
Mar 15, 1996
LAURUS NEEDLE CORE BIOPSY SYSTEM
Gastroenterology & Urology
52d
Cleared
May 12, 1994
DISPOSABLE SUTURE PLACEMENT SYSTEM
General & Plastic Surgery
351d