Kapp Surgical Instrument, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kapp Surgical Instrument, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Michler-Kapp Cardiovascular Vent Catheter
9
Total
9
Cleared
0
Denied
Kapp Surgical Instrument, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Last cleared in 2021. Active since 1984. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kapp Surgical Instrument, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cro Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kapp Surgical Instrument, Inc.
9 devices
Cleared
Jan 28, 2021
Michler-Kapp Cardiovascular Vent Catheter
Cardiovascular
358d
Cleared
Nov 09, 2007
KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536
General & Plastic Surgery
92d
Cleared
Jan 13, 2006
KAPP BARI-RING, MODEL KS-BR-2005
General & Plastic Surgery
332d
Cleared
Aug 08, 2005
MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005
Orthopedic
147d
Cleared
Aug 08, 2005
MONDEAL CONTOUR HO SYSTEM
Orthopedic
147d
Cleared
Jul 28, 2004
KAPP CUSTOM ULNAR HEAD WRIST IMPLANT
Orthopedic
223d
Cleared
Aug 29, 2003
KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT
Orthopedic
218d
Cleared
Nov 08, 1984
COSGROVE MITRAL VALVE RETRACTOR
General & Plastic Surgery
14d
Cleared
Sep 12, 1984
KAPP SPINAL BUTTON
Orthopedic
15d