# Facet Technologies, LLC

- Location (FDA's records): Atlanta, GA
- FDA decisions: 8 (2014–2024): 8 510(k) clearances
- Names in FDA's records: Facet Technologies, LLC (7); Facet Technologies (1)
- Product codes: QRL (3), FMI (3), QRK (1), FMK (1)
- 510(k) review time since 2016: median 74 days, against 93 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ultimed, Inc.: 1 (https://510kreport.com/company/ultimed)
- Novo Nordisk, Inc.: 1 (https://510kreport.com/company/novo-nordisk)
- Becton, Dickinson & CO: 1 (https://510kreport.com/company/becton-dickinson)

## Firms that cite its devices most
- Medipoint Holdings, LLC: 1 (https://510kreport.com/company/medipoint-holdings)
- Medbio, LLC: 1 (https://510kreport.com/company/medbio)

## Its most-cited devices
- K133100: Carefine Pen Needle (2014), cited by 2
- K221433: Facet 28G Universal Lancet (2022), cited by 1
- K140568: Carefine Pen Needle with Quintapoint and Superpoint (2014), cited by 1

## Recent decisions
- K232912: Facet Aurora Reusable Lancet Base (Jan 25, 2024)
- K223370: NeatNick Heel Safety Lancet (Feb 13, 2023)
- K223099: Facet Manatee Reusable Lancing Base (Nov 28, 2022)
- K222539: Facet Blood Lancets (Nov 18, 2022)
- K221433: Facet 28G Universal Lancet (Jul 15, 2022)
- K141749: Carefine Pen Needle Family Including Quintapoint and Superpoint (Jul 29, 2014)
- K140568: Carefine Pen Needle with Quintapoint and Superpoint (May 13, 2014)
- K133100: Carefine Pen Needle (Jan 23, 2014)

Source page: https://510kreport.com/company/facet-technologies