Cleared Traditional

K890682 - OROSPHERE PLUS

K890682 is an FDA 510(k) clearance for OROSPHERE PLUS, manufactured by Jeneric/Pentron, Inc.. The device is a Class 2 Dental device with product code EJJ cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K890682 · Jeneric/Pentron, Inc. · Dental device
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May 1989
Decision
85d
Days
Class 2
Risk

K890682 is an FDA 510(k) clearance for the OROSPHERE PLUS. Classified as Alloy, Amalgam (product code EJJ), Class II - Special Controls.

Submitted by Jeneric/Pentron, Inc. (Wallingford, US). The FDA issued a Cleared decision on May 5, 1989 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3070 - 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 Jeneric/Pentron, Inc. devices

FDA 510(k) Submission Details - K890682

510(k) Number K890682 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 09, 1989
Decision Date May 05, 1989
Days to Decision 85 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
42d faster than avg
Panel avg: 127d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJJ Device Classification - Class 2, Special Controls

Product Code EJJ Alloy, Amalgam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3070
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 - EJJ Alloy, Amalgam

All 25
Devices cleared under the same product code (EJJ) and FDA review panel - the closest regulatory comparables to K890682.
VIVAALLOY HR (AMALGAM)
K901911 · Ivoclar North America, Inc. · Jun 1990
AMALCAP PLUS
K901256 · Ivoclar North America, Inc. · Apr 1990
PENT CAPS
K890662 · Jeneric/Pentron, Inc. · May 1989
OROSPHERE HCDP
K890681 · Jeneric/Pentron, Inc. · May 1989
OLYMPIA ALLOY
K881333 · J.F. Jelenko & Co., Inc. · Apr 1988
HERAEUS' HERAGAM 48, NON GAMMA 2 DEN. AMAL. ALLOY
K875344 · Kulzer, Inc. · Mar 1988