Cleared Traditional

BondEase 2 Topical Skin Adhesive

K243990 · Optmed, Inc. · General & Plastic Surgery
Sep 2025
Decision
267d
Days
Class 2
Risk

About This 510(k) Submission

K243990 is an FDA 510(k) clearance for the BondEase 2 Topical Skin Adhesive, a Tissue Adhesive For The Topical Approximation Of Skin (Class II — Special Controls, product code MPN), submitted by Optmed, Inc. (New York, US). The FDA issued a Cleared decision on September 19, 2025, 267 days after receiving the submission on December 26, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4010.

Submission Details

510(k) Number K243990 FDA.gov
FDA Decision Cleared SESE
Date Received December 26, 2024
Decision Date September 19, 2025
Days to Decision 267 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code MPN — Tissue Adhesive For The Topical Approximation Of Skin
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4010
Definition Docket Number: 2006p-0071 - May 5, 2008 - Reclassified From Class 3 Pma To Class 2 510(k).

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