Innerdyne, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innerdyne, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Innerdyne, Inc. has 12 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 12 cleared submissions from 1995 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innerdyne, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innerdyne, Inc.
12 devices
Cleared
May 26, 2000
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (REVAS)
Cardiovascular
291d
Cleared
Aug 02, 1999
INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE
Gastroenterology & Urology
140d
Cleared
May 18, 1999
INNERDYNE GENERIC RADIALLY EXPANDING DILATION, G-RED DEVICE
General & Plastic Surgery
90d
Cleared
Oct 07, 1998
INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP
General & Plastic Surgery
86d
Cleared
Sep 11, 1998
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (HEPARIN COATED)
Cardiovascular
206d
Cleared
Oct 10, 1997
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM
Cardiovascular
85d
Cleared
Jun 13, 1997
SHERWOOD MEDICAL COMPANY , KANGAROO, ENTRISTAR, PERCUTANEOUS GASTROSTOMY KIT
Gastroenterology & Urology
72d
Cleared
Apr 21, 1997
INNERDYNE STEP TROCAR EXPANABLE PORT, OPEN STEP
General & Plastic Surgery
49d
Cleared
Jul 10, 1996
INNERDYNE STEP TROCAR EXPANDABLE PORT, ONESTEP
General & Plastic Surgery
51d
Cleared
May 28, 1996
INNERDYNE STEP TROCAR EXPANDABLE PORT, MINISTEP
General & Plastic Surgery
43d
Cleared
May 12, 1995
INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP
General & Plastic Surgery
88d
Cleared
May 12, 1995
INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP:
General & Plastic Surgery
88d