Cleared Abbreviated

K150823 - EDLENi Intra-Oral Sensor

K150823 is an FDA 510(k) clearance for EDLENi Intra-Oral Sensor, manufactured by Edlen Imaging, LLC. The device is a Class 2 Radiology device with product code MUH cleared through the Abbreviated 510(k) pathway after a 152-day FDA review.

K150823 · Edlen Imaging, LLC · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2015
Decision
152d
Days
Class 2
Risk

K150823 is an FDA 510(k) clearance for the EDLENi Intra-Oral Sensor. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Edlen Imaging, LLC (Scottsdale, US). The FDA issued a Cleared decision on August 26, 2015 after a review of 152 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Edlen Imaging, LLC devices

FDA 510(k) Submission Details - K150823

510(k) Number K150823 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 27, 2015
Decision Date August 26, 2015
Days to Decision 152 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d slower than avg
Panel avg: 107d · This submission: 152d
Pathway characteristics
Standards-based clearance path.

MUH Device Classification - Class 2, Special Controls

Product Code MUH System, X-ray, Extraoral Source, Digital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 Radiology devices follow this clearance model.

Regulatory Peers - MUH System, X-ray, Extraoral Source, Digital

All 96
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