Lone Star Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lone Star Medical Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Lone Star Medical Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1979 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lone Star Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lone Star Medical Products, Inc.
6 devices
Cleared
Feb 21, 1985
P-3 CLOSING INSTRUMENT
General & Plastic Surgery
45d
Cleared
Jun 05, 1984
SURGICAL ISOLATION BARRIER SYSTEM
General & Plastic Surgery
391d
Cleared
Feb 22, 1982
URETHAL CUTTER CLAMP
Gastroenterology & Urology
48d
Cleared
May 08, 1981
THE SCOTT DIALMENZENSERT
Gastroenterology & Urology
32d
Cleared
Dec 30, 1980
THE INQUINAL RESORVOIR INSERTER
Gastroenterology & Urology
39d
Cleared
Sep 19, 1979
SCOTTS SURGICAL RETRACTOR AND ELASTIC
General & Plastic Surgery
29d