Cleared Traditional

Medipoint Blood Lancets (K223480) - FDA 510(k) Clearance

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K223480 · Medipoint Holdings, LLC · General & Plastic Surgery device
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Jan 2023
Decision
56d
Days
Class 2
Risk

K223480 is an FDA 510(k) clearance for the Medipoint Blood Lancets. Classified as Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature (product code QRK), Class II - Special Controls.

Submitted by Medipoint Holdings, LLC (Mineola, US). The FDA issued a Cleared decision on January 13, 2023 after a review of 56 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4850 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Medipoint Holdings, LLC devices

Submission Details

510(k) Number K223480 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 18, 2022
Decision Date January 13, 2023
Days to Decision 56 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 115d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4850
Definition A Disposable Blood Lancet Intended For A Single Use That Is Comprised Of A Single Use Blade Attached To A Solid, Nonreusable Base That Is Used To Puncture The Skin To Obtain A Drop Of Blood For Diagnostic Purposes.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

All 14
Devices cleared under the same product code (QRK) and FDA review panel - the closest regulatory comparables to K223480.
EasyTouch Lancing Device
K222617 · Stat Medical Devices · Mar 2023
ONE DROP Lancing Device
K223815 · Stat Medical Devices · Feb 2023
Disposable Blood Lancets
K223314 · Huaian Hening Medical Instruments Co., Ltd. · Jan 2023
MedtFine Blood Lancet
K221383 · Shanghai Carelife International Trading Co. , Ltd. · Sep 2022
Disposable Blood Lancet
K221507 · SteriLance Medical (Suzhou), Inc. · Aug 2022
Facet 28G Universal Lancet
K221433 · Facet Technologies, LLC · Jul 2022