Facet Technologies, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 6
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232912 | Facet Aurora Reusable Lancet Base | January 25, 2024 |
| K223370 | NeatNick Heel Safety Lancet | February 13, 2023 |
| K223099 | Facet Manatee Reusable Lancing Base | November 28, 2022 |
| K222539 | Facet Blood Lancets | November 18, 2022 |
| K221433 | Facet 28G Universal Lancet | July 15, 2022 |
| K141749 | CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT | July 29, 2014 |
| K140568 | CAREFINE PEN NEEDLE WITH QUINTAPOINT AND SUPERPOINT | May 13, 2014 |
| K133100 | CAREFINE PEN NEEDLE | January 23, 2014 |