Cleared Traditional

K991844 - PRO-GLASS

K991844 is an FDA 510(k) clearance for PRO-GLASS, manufactured by Cad Cam Ventures. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 54-day FDA review.

K991844 · Cad Cam Ventures · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1999
Decision
54d
Days
Class 2
Risk

K991844 is an FDA 510(k) clearance for the PRO-GLASS. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Cad Cam Ventures (Irving, US). The FDA issued a Cleared decision on July 21, 1999 after a review of 54 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 Cad Cam Ventures devices

FDA 510(k) Submission Details - K991844

510(k) Number K991844 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 1999
Decision Date July 21, 1999
Days to Decision 54 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 127d · This submission: 54d
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 351
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K991844.
CERANA
K992161 · Nordiska Dental AB · Sep 1999
GRAND CERAM
K992023 · Noritake Co., Inc. · Sep 1999
SUPER PORCELAIN TI-22
K992024 · Noritake Co., Inc. · Aug 1999
IPS D.SIGN PORCELAIN
K990817 · Ivoclar North America, Inc. · Apr 1999
VISION PORCELAIN
K990790 · Servo Dental USA, Inc. · Apr 1999
SYMBIOCERAM
K990629 · Ney Dental, Inc. · Mar 1999