Surgrx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgrx, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Surgrx, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 12 cleared submissions from 2003 to 2008.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgrx, Inc.
12 devices
Cleared
Jul 28, 2008
ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD,...
General & Plastic Surgery
98d
Cleared
Sep 27, 2007
ENSEAL TISSUE SEALING DEVICE
General & Plastic Surgery
22d
Cleared
Sep 05, 2007
ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM
General & Plastic Surgery
30d
Cleared
Jul 13, 2007
MODIFICATION TO: ENSEAL PTC TISSUE SEALING DEVICE
General & Plastic Surgery
18d
Cleared
Apr 24, 2007
ENSEAL PTC TISSUE SEALING DEVICE
General & Plastic Surgery
22d
Cleared
Jan 29, 2007
ENSEAL PTC TRIO
General & Plastic Surgery
11d
Cleared
Oct 18, 2006
ENSEAL PTC TISSUE SEATING SEALING DEVICE
General & Plastic Surgery
19d
Cleared
Oct 18, 2006
ENSEAL PTC TISSUE SEALING DEVICE
General & Plastic Surgery
8d
Cleared
Jun 15, 2006
ENSEAL PTC TISSUE SEALING DEVICE
General & Plastic Surgery
13d
Cleared
Apr 01, 2005
ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
General & Plastic Surgery
17d
Cleared
Nov 17, 2004
SURGRX ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
General & Plastic Surgery
16d
Cleared
Jul 03, 2003
SURGRX ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM INCLUDING THE ENSEAL...
General & Plastic Surgery
85d