# K232912: Facet Aurora Reusable Lancet Base

- Pathway: 510(k) (Traditional)
- Applicant: Facet Technologies, LLC
- Decided: Jan 25, 2024 after 128 days
- Product code: QRL (Multiple Use Blood Lancet For Single Patient Use Only)
- Device class: 2
- Regulation: 21 CFR 878.4850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Facet Aurora Reusable Lancet Base (510(k) Exempt): named in the summary without a submission number

## Indications for use
The Facet Aurora Reusable Lancet Base (commonly referred to as a lancing device) is a non-sterile reusable device which provides a spring-loaded mechanism to quickly eject and retract a lancet of proprietary design to effect a lancing event for the purpose of obtaining a droplet of capillary blood for diagnostic testing in children, adolescents, and adults in a home setting. The device is designed to be cleaned and disinfected between uses on a single patient.

Source page: https://510kreport.com/device/K232912
Methodology: https://510kreport.com/methodology