Facet Technologies, LLC
Facet Technologies, LLC holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2024.
Top product codes for Facet Technologies, LLC
Recent clearances by Facet Technologies, LLC
- K232912 — Facet Aurora Reusable Lancet Base
- K223370 — NeatNick Heel Safety Lancet
- K223099 — Facet Manatee Reusable Lancing Base
- K222539 — Facet Blood Lancets
- K221433 — Facet 28G Universal Lancet
- K141749 — CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT
- K140568 — CAREFINE PEN NEEDLE WITH QUINTAPOINT AND SUPERPOINT
Data sourced from openFDA. This site is unofficial and independent of the FDA.