Advance Suture, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advance Suture, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Advance Suture, Inc. has 5 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 5 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Advance Suture, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advance Suture, Inc.
5 devices
Cleared
Jul 26, 1991
ADVANCE SUTURE NONABSORBABLE DACRON SUTURE
General & Plastic Surgery
373d
Cleared
Jul 10, 1991
ADVANCE SUTURE ABSORBABLE GUT SUTURE
General & Plastic Surgery
357d
Cleared
Jun 28, 1991
ADVANCE SUTURE NONABSORBABLE POLYPROPYLENE SUTURE
General & Plastic Surgery
345d
Cleared
Jun 28, 1991
ADVANCE SUTURE NONABSORBABLE NYLON SUTURE
General & Plastic Surgery
345d
Cleared
Jun 28, 1991
ADVANCE SUTURE NONABSORBABLE SILK SUTURE
General & Plastic Surgery
205d