Capillus, LLC is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Capillus, LLC - FDA 510(k) Cleared Devices
Recent clearances: Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352, Capillus302, Capillus312, Capillus352, Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202
7
Total
7
Cleared
0
Denied
Capillus, LLC has 7 FDA 510(k) cleared medical devices. Based in Coral Gables, US.
Historical record: 7 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Capillus, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Capillus, LLC
7 devices
Cleared
Jan 31, 2017
Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302,...
General & Plastic Surgery
78d
Cleared
Nov 18, 2016
Capillus302, Capillus312, Capillus352
General & Plastic Surgery
22d
Cleared
Apr 25, 2016
Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202
General & Plastic Surgery
82d
Cleared
Jan 19, 2016
Capillus202
General & Plastic Surgery
32d
Cleared
Aug 21, 2015
Capillus82
General & Plastic Surgery
77d
Cleared
Jun 09, 2015
Capillus 272 Office Pro
General & Plastic Surgery
92d
Cleared
CT
Jan 29, 2015
Capillus 272 Pro
General & Plastic Surgery
84d