Facet Technologies, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Facet Technologies, LLC has 7 FDA 510(k) cleared medical devices. Based in Kennesaw, US.
Latest FDA clearance: Jan 2024. Active since 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Facet Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Facet Technologies, LLC
7 devices
Cleared
Jan 25, 2024
Facet Aurora Reusable Lancet Base
General & Plastic Surgery
128d
Cleared
Feb 13, 2023
NeatNick Heel Safety Lancet
General & Plastic Surgery
101d
Cleared
Nov 28, 2022
Facet Manatee Reusable Lancing Base
General & Plastic Surgery
59d
Cleared
Nov 18, 2022
Facet Blood Lancets
General & Plastic Surgery
88d
Cleared
Jul 15, 2022
Facet 28G Universal Lancet
General & Plastic Surgery
59d
Cleared
Jul 29, 2014
CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT
General Hospital
29d
Cleared
May 13, 2014
CAREFINE PEN NEEDLE WITH QUINTAPOINT AND SUPERPOINT
General Hospital
69d