Sutures India Pvt., Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Sutures India Pvt., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Sutures India Pvt., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Bangalore, IN.
Historical record: 4 cleared submissions from 2006 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sutures India Pvt., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sutures India Pvt., Ltd.
4 devices
Cleared
Jun 09, 2008
PD SYNTH, ABSORBABLE (POLY DIOXANONE) SUTURE
General & Plastic Surgery
62d
Cleared
Jun 09, 2008
MONOGLYDE, ABSORBABLE (POLIGLECAPRONE 25) SUTURE
General & Plastic Surgery
62d
Cleared
Jun 09, 2008
TRUSYNTH, ABSORBABLE (POLYGLACTIN 910) SUTURE
General & Plastic Surgery
62d
Cleared
Jul 26, 2006
TRULENE MESH
General & Plastic Surgery
203d