Cleared Traditional

K072577 - BISICO IMPRESSION SILICONES & ALGINATES

K072577 is an FDA 510(k) clearance for BISICO IMPRESSION SILICONES & ALGINATES, manufactured by Bisico GmbH & CO KG. The device is a Class 2 Dental device with product code ELW cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K072577 · Bisico GmbH & CO KG · Dental device
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Dec 2007
Decision
83d
Days
Class 2
Risk

K072577 is an FDA 510(k) clearance for the BISICO IMPRESSION SILICONES & ALGINATES. Classified as Material, Impression (product code ELW), Class II - Special Controls.

Submitted by Bisico GmbH & CO KG (Amsterdam, NL). The FDA issued a Cleared decision on December 5, 2007 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3660 - 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 Bisico GmbH & CO KG devices

FDA 510(k) Submission Details - K072577

510(k) Number K072577 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 13, 2007
Decision Date December 05, 2007
Days to Decision 83 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
44d faster than avg
Panel avg: 127d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELW Device Classification - Class 2, Special Controls

Product Code ELW Material, Impression
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3660
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 - ELW Material, Impression

All 266
Devices cleared under the same product code (ELW) and FDA review panel - the closest regulatory comparables to K072577.
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