Cleared Traditional

K261937 - PacTemp Automix NE

K261937 is an FDA 510(k) clearance for PacTemp Automix NE, manufactured by The Belport Company Inc., DBA Gingi-Pak. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K261937 · The Belport Company Inc., DBA Gingi-Pak · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2026
Decision
58d
Days
Class 2
Risk

K261937 is an FDA 510(k) clearance for the PacTemp Automix NE. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by The Belport Company Inc., DBA Gingi-Pak (Camarillo, US). The FDA issued a Cleared decision on August 7, 2026 after a review of 58 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - 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 The Belport Company Inc., DBA Gingi-Pak devices

FDA 510(k) Submission Details - K261937

510(k) Number K261937 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 2026
Decision Date August 07, 2026
Days to Decision 58 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
69d faster than avg
Panel avg: 127d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 421
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