Innerdyne Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innerdyne Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Innerdyne Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 5 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innerdyne Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innerdyne Medical, Inc.
6 devices
Cleared
Oct 11, 1994
INNERDYNE STEP TROCAR EXPANDABLE PORT, S.T.E.P.
General & Plastic Surgery
97d
Cleared
Sep 27, 1994
SINGLE STICK RADIALLY EXPANDING DILATOR
General & Plastic Surgery
92d
Cleared
Apr 25, 1994
INNERDYNE SINGLE-STICK RADIALLY EXPANDING DILATOR
General & Plastic Surgery
84d
Cleared
Apr 18, 1994
INNERDYNE STEP TROCAR EXPANDABLE PORT, S.T.E.P.
General & Plastic Surgery
94d
Cleared
Dec 27, 1993
INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT
General & Plastic Surgery
207d
Cleared
Oct 15, 1993
INTHERM RADIALLY EXPANDING DILATING INTRODUCER
Cardiovascular
204d