Surgrx, Inc. is one of 21815 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgrx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD, ETRIO-314D,-325D,-335D,-345D, ENSEAL UNIVERSAL, ENSEAL TISSUE SEALING DEVICE, ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
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