Scion Medical Technologies, LLC is one of 4723 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Scion Medical Technologies, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Scion Medical Technologies, LLC has 6 FDA 510(k) cleared medical devices. Based in Sauk Centre, US.
Historical record: 6 cleared submissions from 2013 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Scion Medical Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scion Medical Technologies, LLC
6 devices
Cleared
Apr 27, 2017
Star Tissue Marker
General & Plastic Surgery
30d
Cleared
Aug 03, 2016
CASSI II Rotational Core Biopsy System
Gastroenterology & Urology
93d
Cleared
Dec 17, 2015
Beacon Tissue Marker (SE)
General & Plastic Surgery
44d
Cleared
May 20, 2014
GENERAL AND PLASTIC SURGERY
General & Plastic Surgery
48d
Cleared
May 08, 2013
BEACON TISSUE MARKER
General & Plastic Surgery
49d
Cleared
Mar 01, 2013
CASSI II ROTATIONAL CORE BIOPSY SYSTEM
Gastroenterology & Urology
100d