Springfield Surgical Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Springfield Surgical Instruments - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Springfield Surgical Instruments has 8 FDA 510(k) cleared medical devices. Based in Brimfield, US.
Historical record: 8 cleared submissions from 1993 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Springfield Surgical Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Springfield Surgical Instruments
8 devices
Cleared
Sep 29, 1995
BRIMFIELD PRECISION ARTICULATING FAN RETRACTOR
General & Plastic Surgery
71d
Cleared
Jul 26, 1995
BRIMFIELD PRECISION DETACHABLE SCISSOR
General & Plastic Surgery
37d
Cleared
Jan 26, 1995
BRIMFIELD PRECISION GRASPER/DISSECTOR
General & Plastic Surgery
34d
Cleared
Jul 01, 1994
INSULATED SURGICAL ELECTRODE
General & Plastic Surgery
38d
Cleared
Apr 29, 1994
BRIMFIELD PRECISION SECOND GENERATION GRASPER/DISSECTOR
General & Plastic Surgery
43d
Cleared
Apr 22, 1994
BRIMFIELD PRECISION FAN RETRACTOR
General & Plastic Surgery
35d
Cleared
Oct 21, 1993
BRIMFIELD PRECISION SCISSOR
General & Plastic Surgery
101d
Cleared
Oct 15, 1993
BRIMFIELD PRECISION GRASPER/DISSECTOR
General & Plastic Surgery
95d