Cleared Traditional

K981524 - PRILANE

K981524 is an FDA 510(k) clearance for PRILANE, manufactured by Gresco Products, Inc.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K981524 · Gresco Products, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1998
Decision
73d
Days
Class 2
Risk

K981524 is an FDA 510(k) clearance for the PRILANE. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Gresco Products, Inc. (Stafford, US). The FDA issued a Cleared decision on July 10, 1998 after a review of 73 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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 Gresco Products, Inc. devices

FDA 510(k) Submission Details - K981524

510(k) Number K981524 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 1998
Decision Date July 10, 1998
Days to Decision 73 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 127d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 324
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K981524.
OPC LOWWEAR PORCELAIN
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K982664 · Vident · Aug 1998
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K981000 · European Dental Imports, Inc. · May 1998
PROCAD
K980986 · Ivoclar USA, Inc. · May 1998
SONICSYS INLAY
K972648 · Ivoclar North America, Inc. · Oct 1997