510(k) K223099

Device
Facet Manatee Reusable Lancing Base
Applicant
Facet Technologies, LLC
510(k) number
K223099
Product code
QRL
Decision
Substantially Equivalent (SESE)
Decision date
2022-11-28
Date received
2022-09-30
Regulation
878.4850
Classification name
Multiple Use Blood Lancet For Single Patient Use Only
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
James Bonds
Address
3900 N. Commerce Dr. Atlanta GA US 30344 30344

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QRL#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253706Lancing device (HH-XV-T)Tianjin Huahong Technology Co., Ltd.2025-12-09
K250813MICROLET®NEXT 2 Lancing DeviceAscensia Diabetes Care U.S., Inc.2025-05-14
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K232912Facet Aurora Reusable Lancet BaseFacet Technologies, LLC2024-01-25
K231797Medifun Lancing Device, Model No. LD-E1Medifun Corporation2023-11-22
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K221419TD-5010 Lancing Device and TD-5084 Sterile LancetsGostar Co., Ltd.2023-01-20
K222472Lancing System, Sterile Lancet for Single Use, Lancing DeviceShandong Lianfa Medical Plastic Products Co. , Ltd.2022-11-30
K222656LDE4 Lancing DeviceI-Sens, Inc.2022-11-23
K222246Disposable Sterile LancetTianjin Rilifine Medical Device Co., Ltd.2022-11-21
K222539Facet Blood LancetsFacet Technologies, LLC2022-11-18
K221072TRUEdraw Lancing Device, Mini Lancing DeviceTrividia Health2022-10-18
K221175Multi-Lancet Device 2, ReliOn Premier Lancing DeviceArkray, Inc.2022-10-17
K221613Freestyle Lancing Device II, Autolet, Autolet Lite, Unilet LancetsOwen Mumford, Ltd.2022-10-03
K221062RIGHTEST Lancing Device GD500, GE Lancing Device, iGlucose Lancing DeviceBionime Corporation2022-09-26