Cleared Traditional

K952598 - GX-PAN PANORAMIC DENTAL X-RAY SYSTEM

K952598 is an FDA 510(k) clearance for GX-PAN PANORAMIC DENTAL X-RAY SYSTEM, manufactured by Gendex Corp.. The device is a Class 2 Radiology device with product code GEX cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K952598 · Gendex Corp. · Radiology device
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Jun 1995
Decision
23d
Days
Class 2
Risk

K952598 is an FDA 510(k) clearance for the GX-PAN PANORAMIC DENTAL X-RAY SYSTEM. Classified as Powered Laser Surgical Instrument within the GEX classification (a category for powered laser surgical instruments across multiple specialties), Class II - Special Controls.

Submitted by Gendex Corp. (Des Plaines, US). The FDA issued a Cleared decision on June 29, 1995 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 878.4810 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Gendex Corp. devices

FDA 510(k) Submission Details - K952598

510(k) Number K952598 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 1995
Decision Date June 29, 1995
Days to Decision 23 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 107d · This submission: 23d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEX Device Classification - Class 2, Special Controls

Product Code GEX Powered Laser Surgical Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4810
Definition A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light.
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 - GEX Powered Laser Surgical Instrument

All 2435
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K952598.
MEGABEAM ENDO-ENT PROBE
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K952340 · Ceram Optec, Inc. · Jun 1995
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K951204 · Sharplan Lasers, Inc. · Jun 1995