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	<title>Surgical Product Guide &#187; Laparoscopy</title>
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	<link>http://blog.surgicalproductguide.com</link>
	<description>A comprehensive guide to surgical products for medical professionals </description>
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		<title>FDA Clears Marketing of PatchAssist Laparoscopic Hernia Mesh Placement Device</title>
		<link>http://blog.surgicalproductguide.com/2010/07/08/fda-clears-marketing-of-patchassist-laparoscopic-hernia-mesh-placement-device/</link>
		<comments>http://blog.surgicalproductguide.com/2010/07/08/fda-clears-marketing-of-patchassist-laparoscopic-hernia-mesh-placement-device/#comments</comments>
		<pubDate>Thu, 08 Jul 2010 20:44:37 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[hernia]]></category>
		<category><![CDATA[laparoscopic hernia mesh]]></category>
		<category><![CDATA[PatchAssist]]></category>
		<category><![CDATA[PolyTouch Medical]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/?p=235</guid>
		<description><![CDATA[Israel&#8217;s PolyTouch Medical has received FDA clearance to market its PatchAssist laparoscopic hernia mesh placement device. The tool was developed to allow surgeons a more predictable and standardized approach to apply hernia patches. PatchAssist easily unfolds the mesh inside the abdominal cavity, accurately places the mesh over the hernia defect and enables surgeon to verify [...]]]></description>
			<content:encoded><![CDATA[<p>Israel&#8217;s PolyTouch Medical has received FDA clearance to market its PatchAssist laparoscopic hernia mesh placement device. The tool was developed to allow surgeons a more predictable and standardized approach to apply hernia patches. PatchAssist easily unfolds the mesh inside the abdominal cavity, accurately places the mesh over the hernia defect and enables surgeon to verify the mesh position before attachment is made. Patch Assist does not change laparoscopic techniques used today by surgeons, rather it eliminates manual, complicated, and time consuming tasks.</p>
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		<title>PolyTouch Medical Ltd. Receives FDA Clearance to Commercialize PatchAssist(TM)</title>
		<link>http://blog.surgicalproductguide.com/2010/06/23/polytouch-medical-ltd-receives-fda-clearance-to-commercialize-patchassisttm/</link>
		<comments>http://blog.surgicalproductguide.com/2010/06/23/polytouch-medical-ltd-receives-fda-clearance-to-commercialize-patchassisttm/#comments</comments>
		<pubDate>Wed, 23 Jun 2010 09:56:53 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[Surgical Instruments]]></category>
		<category><![CDATA[FDA 510(k) clearance]]></category>
		<category><![CDATA[laparoscopic]]></category>
		<category><![CDATA[laparoscopic ventral hernia repair]]></category>
		<category><![CDATA[PatchAssist(TM)]]></category>
		<category><![CDATA[PolyTouch Medical Ltd]]></category>
		<category><![CDATA[prosthetic placement technologies]]></category>
		<category><![CDATA[soft tissue]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/?p=222</guid>
		<description><![CDATA[PolyTouch Medical Ltd. has announced that it has received broad FDA 510(k) clearance to commercialize PatchAssist(TM). PatchAssist is an innovative laparoscopic surgical instrument that enables accurate and rapid delivery and placement of soft tissue prosthetics for a variety of procedures, including laparoscopic ventral hernia repair (LVHR). PatchAssist enables surgeons to rapidly deliver and position soft [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blog.surgicalproductguide.com/files/2010/06/PolyTouch-Medical-Ltd.png"><img class="alignright size-full wp-image-223" style="margin: 5px" src="http://blog.surgicalproductguide.com/files/2010/06/PolyTouch-Medical-Ltd.png" border="0" alt="PolyTouch Medical Ltd" width="200" height="72" /></a>PolyTouch Medical Ltd. has announced that it has received broad FDA 510(k) clearance to commercialize PatchAssist(TM). PatchAssist is an innovative laparoscopic surgical instrument that enables accurate and rapid delivery and placement of soft tissue prosthetics for a variety of procedures, including laparoscopic ventral hernia repair (LVHR). PatchAssist enables surgeons to rapidly deliver and position soft tissue prosthetics over the defect potentially reducing operation time by 30% &#8211; 50%.</p>
<p>Read the full story <a href="http://www.sys-con.com/node/1438564" target="_blank">here</a></p>
<div style="width: 1px;height: 1px;overflow: hidden"><!--[if gte mso 9]&gt;  Normal 0   false false false         MicrosoftInternetExplorer4  &lt;![endif]--><!--[if gte mso 9]&gt;   &lt;![endif]--><!--  /* Font Definitions */  @font-face 	{font-family:"MS Mincho"; 	panose-1:2 2 6 9 4 2 5 8 3 4; 	mso-font-alt:"ＭＳ 明朝"; 	mso-font-charset:128; 	mso-generic-font-family:roman; 	mso-font-format:other; 	mso-font-pitch:fixed; 	mso-font-signature:1 134676480 16 0 131072 0;} @font-face 	{font-family:"\@MS Mincho"; 	panose-1:0 0 0 0 0 0 0 0 0 0; 	mso-font-charset:128; 	mso-generic-font-family:roman; 	mso-font-format:other; 	mso-font-pitch:fixed; 	mso-font-signature:1 134676480 16 0 131072 0;}  /* Style Definitions */  p.MsoNormal, li.MsoNormal, div.MsoNormal 	{mso-style-parent:""; 	margin:0in; 	margin-bottom:.0001pt; 	mso-pagination:widow-orphan; 	font-size:12.0pt; 	font-family:"Times New Roman"; 	mso-fareast-font-family:"MS Mincho";} @page Section1 	{size:8.5in 11.0in; 	margin:1.0in 1.25in 1.0in 1.25in; 	mso-header-margin:.5in; 	mso-footer-margin:.5in; 	mso-paper-source:0;} div.Section1 	{page:Section1;} --><!--[if gte mso 10]&gt; &lt;!   /* Style Definitions */  table.MsoNormalTable 	{mso-style-name:&quot;Table Normal&quot;; 	mso-tstyle-rowband-size:0; 	mso-tstyle-colband-size:0; 	mso-style-noshow:yes; 	mso-style-parent:&quot;&quot;; 	mso-padding-alt:0in 5.4pt 0in 5.4pt; 	mso-para-margin:0in; 	mso-para-margin-bottom:.0001pt; 	mso-pagination:widow-orphan; 	font-size:10.0pt; 	font-family:&quot;Times New Roman&quot;; 	mso-fareast-font-family:&quot;Times New Roman&quot;; 	mso-ansi-language:#0400; 	mso-fareast-language:#0400; 	mso-bidi-language:#0400;} --> <!--[endif]--><span>PolyTouch Medical Ltd. has announced that it has received broad FDA 510(k) clearance to commercialize PatchAssist(TM). PatchAssist is an innovative laparoscopic surgical instrument that enables accurate and rapid delivery and placement of soft tissue prosthetics for a variety of procedures, including laparoscopic ventral hernia repair (LVHR). PatchAssist enables surgeons to rapidly deliver and position soft tissue prosthetics over the defect potentially reducing operation time by 30% &#8211; 50%.</span></div>
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		<title>Bovie laparoscopic SEER device approved</title>
		<link>http://blog.surgicalproductguide.com/2009/10/15/bovie-laparoscopic-seer-device-approved/</link>
		<comments>http://blog.surgicalproductguide.com/2009/10/15/bovie-laparoscopic-seer-device-approved/#comments</comments>
		<pubDate>Fri, 16 Oct 2009 03:51:48 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[Bovie Medical]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[kidney surgery]]></category>
		<category><![CDATA[SEER device]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/?p=144</guid>
		<description><![CDATA[Bovie Medical Corp has received clearance to sell a device that cuts and reseals tissue in kidney surgeries. The FDA has approved market of Bovie&#8217;s laparoscopic SEER device, which is used for cutting and coagulating soft tissue. It is intended to be used in partial removal of kidneys. Bovie said the laparoscopic SEER, or Saline [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blog.surgicalproductguide.com/files/2009/10/Bovie1.png"><img class="alignleft size-full wp-image-145" style="margin: 5px" src="http://blog.surgicalproductguide.com/files/2009/10/Bovie1.png" alt="Bovie1" width="200" height="32" /></a>Bovie Medical Corp has received clearance to sell a device that cuts and reseals tissue in kidney surgeries. The FDA has approved market of Bovie&#8217;s laparoscopic SEER device, which is used for cutting and coagulating soft tissue. It is intended to be used in partial removal of kidneys. Bovie said the laparoscopic SEER, or Saline Enhance Electrosurgical Resection, device is an extension a line the company launched earlier this year.</p>
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		<title>Virtual Ports EndoGrab device receives CE Mark</title>
		<link>http://blog.surgicalproductguide.com/2009/08/20/virtual-ports-endograb-device-receives-ce-mark/</link>
		<comments>http://blog.surgicalproductguide.com/2009/08/20/virtual-ports-endograb-device-receives-ce-mark/#comments</comments>
		<pubDate>Fri, 21 Aug 2009 04:27:01 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[CE Mark]]></category>
		<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[EndoGrab]]></category>
		<category><![CDATA[laparoscopic]]></category>
		<category><![CDATA[laparoscopic surgery]]></category>
		<category><![CDATA[Virtual Ports]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/?p=114</guid>
		<description><![CDATA[Virtual Ports Ltd has obtained EU CE Mark for its EndoGrab device that reduces the number of incisions (or ports) needed to perform laparoscopic surgical procedures. EndoGrab is an internally anchored, hands-free retracting device that eliminates the need for the hand-held retractor that is traditionally used during laparoscopic procedures. This would reduce scarring and some [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blog.surgicalproductguide.com/files/2009/08/VirtualPorts.png"><img class="alignleft size-full wp-image-115" style="margin: 5px" src="http://blog.surgicalproductguide.com/files/2009/08/VirtualPorts.png" alt="VirtualPorts" width="200" height="115" /></a>Virtual Ports Ltd has obtained EU CE Mark for its EndoGrab device that reduces the number of incisions (or ports) needed to perform laparoscopic surgical procedures. EndoGrab is an internally anchored, hands-free retracting device that eliminates the need for the hand-held retractor that is traditionally used during laparoscopic procedures. This would reduce scarring and some of post-surgical complications associated with abdominal incisions.</p>
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		<item>
		<title>Study depicts 98.8% survival rate through laparoscopy-assisted surgery</title>
		<link>http://blog.surgicalproductguide.com/2009/07/10/study-depicts-988-survival-rate-through-laparoscopy-assisted-surgery/</link>
		<comments>http://blog.surgicalproductguide.com/2009/07/10/study-depicts-988-survival-rate-through-laparoscopy-assisted-surgery/#comments</comments>
		<pubDate>Fri, 10 Jul 2009 05:01:25 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[Post Operative]]></category>
		<category><![CDATA[Research]]></category>
		<category><![CDATA[gastric cancer]]></category>
		<category><![CDATA[Laparoscopic gastrectomy]]></category>
		<category><![CDATA[laparoscopy-assisted surgery]]></category>
		<category><![CDATA[surgical incisions]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/2009/07/10/study-depicts-988-survival-rate-through-laparoscopy-assisted-surgery/</guid>
		<description><![CDATA[A study published in the June 2009 issue of the Archives of Surgery depicted that laparoscopy-assisted surgery for early gastric cancer resulted in a 98.8% three-year overall survival rate in patients with early gastric cancer. Laparoscopic gastrectomy is a minimally invasive surgical procedure, in contrast with the total removal of the lymph nodes in traditional [...]]]></description>
			<content:encoded><![CDATA[<p><img src="http://blog.surgicalproductguide.com/files/2009/07/aos.png" hspace="5" height="69" width="200" vspace="5" align="right" />A study published in the June 2009 issue of the Archives of Surgery depicted that laparoscopy-assisted surgery for early gastric cancer resulted in a 98.8% three-year overall survival rate in patients with early gastric cancer. Laparoscopic gastrectomy is a minimally invasive surgical procedure, in contrast with the total removal of the lymph nodes in traditional treatment. In Laparoscopic gastrectomy, a surgeon removes the stomach through a lighted tube, eliminating the need for large surgical incisions and possibly reducing the risk of infection, healing complications, pain and blood loss.</p>
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		<item>
		<title>Covidien receives FDA nod for surgery kit for laparoscopic procedures</title>
		<link>http://blog.surgicalproductguide.com/2008/06/24/covidien-receives-fda-nod-for-surgery-kit-for-laparoscopic-procedures/</link>
		<comments>http://blog.surgicalproductguide.com/2008/06/24/covidien-receives-fda-nod-for-surgery-kit-for-laparoscopic-procedures/#comments</comments>
		<pubDate>Tue, 24 Jun 2008 21:08:44 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Laparoscopy]]></category>
		<category><![CDATA[Covidien]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[laparoscopic procedure]]></category>
		<category><![CDATA[SILS Procedure Kits]]></category>
		<category><![CDATA[surgery kit]]></category>
		<guid isPermaLink="false">http://www.surgicalproductguide.com/blog/2008/06/24/covidien-receives-fda-nod-for-surgery-kit-for-laparoscopic-procedures/</guid>
		<description><![CDATA[Covidien Ltd. has received approval from the FDA to market a surgery kit for use in laparoscopic procedures. Covidien&#8217;s SILS Procedure Kits can be used by surgeons to perform the procedures through a single incision through a patient&#8217;s belly button. The kit is set for launch this summer.]]></description>
			<content:encoded><![CDATA[<p><img vspace="5" align="right" width="200" src="http://blog.surgicalproductguide.com/files/2008/05/covidien.png" hspace="5" alt="Covidien" height="60" /><a href="http://www.covidien.com/covidien/pagebuilder.aspx?webPageID=161206&amp;websiteID=161199">Covidien Ltd.</a> has received approval from the FDA to market a surgery kit for use in laparoscopic procedures. Covidien&#8217;s SILS Procedure Kits can be used by surgeons to perform the procedures through a single incision through a patient&#8217;s belly button. The kit is set for launch this summer.</p>
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