Cleared Traditional

cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200)

K251852 · VPIX Medical, Inc. · General & Plastic Surgery
Feb 2026
Decision
241d
Days
Class 2
Risk

About This 510(k) Submission

K251852 is an FDA 510(k) clearance for the cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200), a Confocal Optical Imaging (Class II — Special Controls, product code OWN), submitted by VPIX Medical, Inc. (Daejeon, KR). The FDA issued a Cleared decision on February 13, 2026, 241 days after receiving the submission on June 17, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K251852 FDA.gov
FDA Decision Cleared SESE
Date Received June 17, 2025
Decision Date February 13, 2026
Days to Decision 241 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OWN — Confocal Optical Imaging
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition Collection Of Light Signals For Visualization Of Cellular Microstructures.

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