Cleared Traditional

3M Filtek Supreme Flowable Restorative (K221695) - FDA 510(k) Clearance

Class II Dental device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K221695 · 3M Company Espe Dental Products · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2022
Decision
3d
Days
Class 2
Risk

K221695 is an FDA 510(k) clearance for the 3M Filtek Supreme Flowable Restorative. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by 3M Company Espe Dental Products (Saint Paul, US). The FDA issued a Cleared decision on June 13, 2022 after a review of 3 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 3M Company Espe Dental Products devices

Submission Details

510(k) Number K221695 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 2022
Decision Date June 13, 2022
Days to Decision 3 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
124d faster than avg
Panel avg: 127d · This submission: 3d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

Device Classification

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 Consultant

Regulatory Technology Services, LLC
Prithul Bom

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - EBF Material, Tooth Shade, Resin

All 291
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K221695.
G-CAM
K220329 · Graphenano Dental S.L. · Aug 2022
IMICRYL Composite, Composite Flow Materials
K220077 · Imicryl Dis Malzemeleri Sanayi VE Ticaret AS · Aug 2022
J-Temp
K221909 · Ultradent Products, Inc. · Jul 2022
OptiComp
K202920 · Pac-Dent, Inc. · May 2022
Venus Bulk Flow ONE
K220605 · Kulzer, LLC · Apr 2022
Saremco Print CROWNTEC
K213343 · Saremco Dental AG · Jan 2022