Cleared Traditional

K043131 - TORPICALGIN

K043131 is an FDA 510(k) clearance for TORPICALGIN, manufactured by Zhermack S.P.A.. The device is a Class 2 Dental device with product code ELW cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K043131 · Zhermack S.P.A. · Dental device
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Dec 2004
Decision
33d
Days
Class 2
Risk

K043131 is an FDA 510(k) clearance for the TORPICALGIN. Classified as Material, Impression (product code ELW), Class II - Special Controls.

Submitted by Zhermack S.P.A. (Bend, US). The FDA issued a Cleared decision on December 15, 2004 after a review of 33 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 Zhermack S.P.A. devices

FDA 510(k) Submission Details - K043131

510(k) Number K043131 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 12, 2004
Decision Date December 15, 2004
Days to Decision 33 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
94d faster than avg
Panel avg: 127d · This submission: 33d
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 237
Devices cleared under the same product code (ELW) and FDA review panel - the closest regulatory comparables to K043131.
FUSION FAST
K043471 · GC America, Inc. · Jan 2005
HYDROGUM SOFT
K043118 · Zhermack S.P.A. · Jan 2005
FLEXITIME XTREME
K042878 · Heraeus Kulzer, Inc. · Dec 2004
GC FUSION
K041398 · GC America, Inc. · Jun 2004
MULTIPLE (ADDITION SILICONE IMPRESSION MATERIAL)
K041229 · Cosmedent, Inc. · Jun 2004
CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL
K041028 · Crown Delta Corp. · May 2004