Cleared Traditional

K881903 - PROSTHODENT VL

K881903 is an FDA 510(k) clearance for PROSTHODENT VL, manufactured by Lee Pharmaceuticals. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K881903 · Lee Pharmaceuticals · Dental device
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Jul 1988
Decision
56d
Days
Class 2
Risk

K881903 is an FDA 510(k) clearance for the PROSTHODENT VL. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Lee Pharmaceuticals (South El Monte, US). The FDA issued a Cleared decision on July 1, 1988 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Lee Pharmaceuticals devices

FDA 510(k) Submission Details - K881903

510(k) Number K881903 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1988
Decision Date July 01, 1988
Days to Decision 56 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 127d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 800
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K881903.
VISIO-PERL
K882566 · Espe GmbH (Us) · Oct 1988
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K883392 · Scientific Pharmaceuticals, Inc. · Oct 1988
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CLEARFIL PHOTO CORE
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G-CERA PORCELAIN BOND
K880765 · G-C Intl. Corp. · Apr 1988
PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST
K875313 · Bisco, Inc. · Mar 1988