Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NeatNick Heel Safety Lancet

K-Number: K223370 · 2023-02-13

ApplicantFacet Technologies, LLC
Decision Date2023-02-13
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NeatNick Heel Safety Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Facet Technologies, LLC. It received FDA 510(k) clearance on 2023-02-13 under 510(k) number K223370. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeatNick Heel Safety Lancet?

NeatNick Heel Safety Lancet is a medical device that received FDA 510(k) clearance on 2023-02-13. The listed applicant is Facet Technologies, LLC. The 510(k) number is K223370.

When did NeatNick Heel Safety Lancet receive FDA 510(k) clearance?

NeatNick Heel Safety Lancet received FDA 510(k) clearance on 2023-02-13, under 510(k) number K223370.

Who is the listed applicant for NeatNick Heel Safety Lancet?

The FDA 510(k) record lists Facet Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NeatNick Heel Safety Lancet?

The FDA product code for NeatNick Heel Safety Lancet is FMK.

Other records listing Facet Technologies, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232912Facet Aurora Reusable Lancet BaseK223099Facet Manatee Reusable Lancing BaseK222539Facet Blood LancetsK221433Facet 28G Universal Lancet

Related Devices (Code: FMK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261045Verifine Safety LancetsPromisemed Hangzhou Meditech Co., Ltd.K260191Safety lancet (XXXVII)Tianjin Huahong Technology Co., Ltd.K253605Safety Heel LancetNingbo Medsun Medical Co., Ltd.K252490Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)Tianjin Huahong Technology Co., Ltd.K251694safety lancetTianjin Huahong Technology Co., Ltd.K244036Heel Incision Safety Lancet (SteriHeel 2)SteriLance Medical (Suzhou), Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑