Cleared Traditional

K243796 - GLOVEONE Powder-Free Nitrile Examinatio...

K243796 is an FDA 510(k) clearance for GLOVEONE Powder-Free Nitrile Examinatio..., manufactured by Glove One, LLC. The device is a Class 1 General Hospital device with product code LZA cleared through the Traditional 510(k) pathway after a 175-day FDA review.

K243796 · Glove One, LLC · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2025
Decision
175d
Days
Class 1
Risk

K243796 is an FDA 510(k) clearance for the GLOVEONE™ Powder-Free Nitrile Examination Gloves – Non-sterile [Tested for us.... Classified as Polymer Patient Examination Glove (product code LZA), Class I - General Controls.

Submitted by Glove One, LLC (Mooresville, US). The FDA issued a Cleared decision on June 3, 2025 after a review of 175 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6250 - the FDA general hospital 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Glove One, LLC devices

FDA 510(k) Submission Details - K243796

510(k) Number K243796 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 2024
Decision Date June 03, 2025
Days to Decision 175 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d slower than avg
Panel avg: 129d · This submission: 175d
Pathway characteristics
Predicate-based equivalence.

LZA Device Classification - Class 1, General Controls

Product Code LZA Polymer Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Nitrile (or Polymer) Patient Examination Glove Is A Disposable Device Made Of Nitrile Rubber Or Synthetic Polymers That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Consultant

Terrie M Heidemann
Terrie M Heidemann

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - LZA Polymer Patient Examination Glove

All 684
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