Cleared Traditional

K810266 - ETCHING GEL

K810266 is an FDA 510(k) clearance for ETCHING GEL, manufactured by Espe-Premier Sales Co.. The device is a Class 2 Dental device with product code EJK cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K810266 · Espe-Premier Sales Co. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1981
Decision
21d
Days
Class 2
Risk

K810266 is an FDA 510(k) clearance for the ETCHING GEL. Classified as Liner, Cavity, Calcium Hydroxide (product code EJK), Class II - Special Controls.

Submitted by Espe-Premier Sales Co. (Walker, US). The FDA issued a Cleared decision on February 23, 1981 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3250 - 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 Espe-Premier Sales Co. devices

FDA 510(k) Submission Details - K810266

510(k) Number K810266 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 1981
Decision Date February 23, 1981
Days to Decision 21 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
107d faster than avg
Panel avg: 128d · This submission: 21d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJK Device Classification - Class 2, Special Controls

Product Code EJK Liner, Cavity, Calcium Hydroxide
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3250
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 - EJK Liner, Cavity, Calcium Hydroxide

All 61
Devices cleared under the same product code (EJK) and FDA review panel - the closest regulatory comparables to K810266.
KERR SEALAPEX ROOT CANAL SEALER
K841910 · Sybron Corp. · Jul 1984
NU-CAP CALCIUM HYDROX. PULP CAPPING
K831575 · Coe Laboratories, Inc. · Jun 1983
IMPROVED DYCAL
K820215 · Dentsply Intl. · Mar 1982
REOLIT
K802685 · Vivadent (Usa), Inc. · Nov 1980
MONOJECT PULP-CAPPING MATERIAL
K791088 · Sherwood Medical Co. · Oct 1979
LINER, CAVITY CALCIUM HYDROXIDE
K781688 · Kerr Corporation (Danbury) · Dec 1978