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   <title>Saluda Medical Announces First U.S. Surgical Cases Using Newly Approved CAP24™ Paddle Lead</title>
   <link>http://www.streetinsider.com/Press+Releases/Saluda+Medical+Announces+First+U.S.+Surgical+Cases+Using+Newly+Approved+CAP24%E2%84%A2+Paddle+Lead/26777730.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 16, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial‑stage medical device company advancing closed‑loop neuromodulation for chronic neurological conditions, today announced the first &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. surgical cases using the newly FDA‑approved Evoke® CAP24™ paddle lead.&lt;/p&gt;
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   <title>Saluda Medical Announces First U.S. Surgical Cases Using Newly Approved CAP24™ Paddle Lead</title>
   <link>http://www.streetinsider.com/PRNewswire/Saluda+Medical+Announces+First+U.S.+Surgical+Cases+Using+Newly+Approved+CAP24%E2%84%A2+Paddle+Lead/26777730.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 16, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial‑stage medical device company advancing closed‑loop neuromodulation for chronic neurological conditions, today announced the first &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. surgical cases using the newly FDA‑approved Evoke® CAP24™ paddle lead.&lt;/p&gt;
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   <title>FDA clears Saluda Medical's CAP24 paddle lead for spinal cord stimulation</title>
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&lt;p&gt;Saluda Medical (ASX: SLD) announced that the U.S. Food and Drug Administration has approved its CAP24 surgical paddle lead, allowing the device to be marketed and sold in the United States.&lt;/p&gt;

&lt;p&gt;The CAP24 is a paddle lead designed for use with Saluda's Evoke System and EVA Sensing Technology in spinal cord stimulation (SCS) procedures. Paddle leads are an alternative to percutaneous leads and are generally preferred by neurosurgeons and orthopedic surgeons, who account for approximately 30% of all SCS implants in the U.S., according to the company.&lt;/p&gt;

&lt;p&gt;The device features a 24-electrode, three-column configuration and is designed to sense and measure evoked</description>
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   <pubDate>Tue, 30 Jun 2026 09:15:17 -0400</pubDate>
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   <title>FDA clears Saluda Medical's CAP24 paddle lead for spinal cord stimulation</title>
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&lt;p&gt;Saluda Medical (ASX: SLD) announced that the U.S. Food and Drug Administration has approved its CAP24 surgical paddle lead, allowing the device to be marketed and sold in the United States.&lt;/p&gt;

&lt;p&gt;The CAP24 is a paddle lead designed for use with Saluda's Evoke System and EVA Sensing Technology in spinal cord stimulation (SCS) procedures. Paddle leads are an alternative to percutaneous leads and are generally preferred by neurosurgeons and orthopedic surgeons, who account for approximately 30% of all SCS implants in the U.S., according to the company.&lt;/p&gt;

&lt;p&gt;The device features a 24-electrode, three-column configuration and is designed to sense and measure evoked</description>
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   <title>FDA clears Saluda Medical's CAP24 paddle lead for spinal cord stimulation</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Saluda+Medical%27s+CAP24+paddle+lead+for+spinal+cord+stimulation/26710968.html</link>
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&lt;p&gt;Saluda Medical (ASX: SLD) announced that the U.S. Food and Drug Administration has approved its CAP24 surgical paddle lead, allowing the device to be marketed and sold in the United States.&lt;/p&gt;

&lt;p&gt;The CAP24 is a paddle lead designed for use with Saluda's Evoke System and EVA Sensing Technology in spinal cord stimulation (SCS) procedures. Paddle leads are an alternative to percutaneous leads and are generally preferred by neurosurgeons and orthopedic surgeons, who account for approximately 30% of all SCS implants in the U.S., according to the company.&lt;/p&gt;

&lt;p&gt;The device features a 24-electrode, three-column configuration and is designed to sense and measure evoked</description>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/Press+Releases/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/Press+Releases/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <pubDate>Tue, 30 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/Press+Releases/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <pubDate>Tue, 30 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/PRNewswire/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <pubDate>Tue, 30 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/PRNewswire/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <title>Saluda Medical Receives U.S. FDA Approval for New CAP24™ Surgical Paddle Lead</title>
   <link>http://www.streetinsider.com/PRNewswire/Saluda+Medical+Receives+U.S.+FDA+Approval+for+New+CAP24%E2%84%A2+Surgical+Paddle+Lead/26710957.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.bloton&quot; idsrc=&quot;xmltag.org&quot; &gt;BLOOMINGTON, Minn.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX: SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (&quot;FDA&quot;) has approved Saluda's CAP24 paddle lead, allowing it to be marketed and sold in the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Paddle leads are an alternative to percutaneous leads and this approval enables the Company to target neurosurgeons and orthopedic surgeons, who generally prefer the surgical</description>
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   <title>Saluda Medical Receives Regulatory Approval for EVA™ Sensing Technology in Europe with recognition in Australia</title>
   <link>http://www.streetinsider.com/Press+Releases/Saluda+Medical+Receives+Regulatory+Approval+for+EVA%E2%84%A2+Sensing+Technology+in+Europe+with+recognition+in+Australia/25822250.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.mn.minnea&quot; idsrc=&quot;xmltag.org&quot; &gt;MINNEAPOLIS&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Jan. 8, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Australia:SLD&quot; idsrc=&quot;xmltag.org&quot; &gt;Saluda Medical, Inc.&lt;/span&gt; (ASX:SLD, &quot;Saluda&quot; or the &quot;Company&quot;), a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed-loop neuromodulation platform, announced that, as expected, its next-generation EVA™ Sensing Technology has now received CE certification for &lt;span&gt;commercialization &lt;/span&gt;in &lt;location value=&quot;LR/eur&quot; idsrc=&quot;xmltag.org&quot; &gt;Europe&lt;/location&gt; with recognition of this approval in &lt;location value=&quot;LC/au&quot; idsrc=&quot;xmltag.org&quot; &gt;Australia&lt;/location&gt;. This follows FDA approval of EVA in &lt;chron&gt;December 2024&lt;/chron&gt;.&lt;/p&gt;
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   <pubDate>Thu, 08 Jan 2026 05:00:00 -0400</pubDate>
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   <title>Saluda Medical Receives Regulatory Approval for EVA™ Sensing Technology in Europe with recognition in Australia</title>
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   <pubDate>Thu, 08 Jan 2026 05:00:00 -0400</pubDate>
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