Cleared Traditional

K011762 - HI-WAVE

Also marketed or referenced as:
POUR-PLUS

K011762 is an FDA 510(k) clearance for HI-WAVE, manufactured by Denplus, Inc.. The device is a Class 2 Dental device with product code EBI cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K011762 · Denplus, Inc. · Dental device
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Aug 2001
Decision
77d
Days
Class 2
Risk

K011762 is an FDA 510(k) clearance for the HI-WAVE. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.

Submitted by Denplus, Inc. (Longueuil, Quebec, CA). The FDA issued a Cleared decision on August 23, 2001 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3760 - the FDA dental device regulatory 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 Denplus, Inc. devices

FDA 510(k) Submission Details - K011762

510(k) Number K011762 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 2001
Decision Date August 23, 2001
Days to Decision 77 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 127d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBI Device Classification - Class 2, Special Controls

Product Code EBI Resin, Denture, Relining, Repairing, Rebasing
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3760
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 Dental devices follow this clearance model.

Regulatory Peers - EBI Resin, Denture, Relining, Repairing, Rebasing

All 215
Devices cleared under the same product code (EBI) and FDA review panel - the closest regulatory comparables to K011762.
TOKUYAMA REBASE II
K022641 · Tokuyama America, Inc. · Oct 2002
SECURE SOFT
K021437 · Imtec Corp. · Jul 2002
SECURE RELINE/PICKUP MATERIAL
K021586 · Imtec Corp. · Jun 2002
TRUBYTE DENTURE BASE RESIN SYSTEM
K011560 · Dentsply Intl. · Jul 2001
HARD RELINER
K011277 · S & C Polymer GmbH · Jun 2001
VERSYO.COM
K010800 · Heraeus Kulzer, Inc. · May 2001