Cleared Traditional

K032797 - DELIGHT DENTAL ER: YAG LASER SYSTEM

K032797 is an FDA 510(k) clearance for DELIGHT DENTAL ER: YAG LASER SYSTEM, manufactured by Hoya Photonics, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 210-day FDA review.

K032797 · Hoya Photonics, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2004
Decision
210d
Days
Class 2
Risk

K032797 is an FDA 510(k) clearance for the DELIGHT DENTAL ER: YAG LASER 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 Hoya Photonics, Inc. (Fremont, US). The FDA issued a Cleared decision on April 5, 2004 after a review of 210 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4810 - the FDA general and plastic surgery 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 & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Hoya Photonics, Inc. devices

FDA 510(k) Submission Details - K032797

510(k) Number K032797 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 2003
Decision Date April 05, 2004
Days to Decision 210 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d slower than avg
Panel avg: 115d · This submission: 210d
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEX Powered Laser Surgical Instrument

All 1812
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K032797.
PHOTOSILK PULSED LIGHT SYSTEM
K041095 · Cynosure, Inc. · May 2004
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K040289 · Cynosure, Inc. · Apr 2004
COOLTOUCH
K040131 · New Star Lasers, Inc. · Apr 2004
PALOMAR LUXV HANDPIECE
K040081 · Palomar Medical Technologies, Inc. · Apr 2004
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K034011 · Laserscope · Mar 2004
PROFILE 2000/3000 LASER SYSTEM
K040005 · Sciton, Inc · Mar 2004