Cleared Traditional

K241314 - KLS Martin Oral-Max Implants MR Conditional (bundled) (FDA 510(k) Clearance)

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

K241314 · KLS-Martin L.P. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2024
Decision
98d
Days
Class 2
Risk

K241314 is an FDA 510(k) clearance for the KLS Martin Oral-Max Implants MR Conditional (bundled). Classified as Plate, Bone (product code JEY), Class II - Special Controls.

Submitted by KLS-Martin L.P. (Jacksonville, US). The FDA issued a Cleared decision on August 16, 2024 after a review of 98 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4760 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all KLS-Martin L.P. devices

Submission Details

510(k) Number K241314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 2024
Decision Date August 16, 2024
Days to Decision 98 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
29d faster than avg
Panel avg: 127d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JEY Plate, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.4760
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 - JEY Plate, Bone

All 291
Devices cleared under the same product code (JEY) and FDA review panel - the closest regulatory comparables to K241314.
Leforte MMF System
K252246 · Jeil Medical Corporation · Apr 2026
Southern Craniomaxillofacial (CMF) System
K253373 · Southern Medical (Pty) , Ltd. · Dec 2025
Inion CPS 1.5 Baby Bioabsorbable Fixation System
K251441 · Inion OY · Nov 2025
MRI Universal
K240651 · Stryker Leibinger GmbH & Co KG · Jul 2024
tmCMF Solution
K233874 · Techmah Cmf · Jul 2024
METICULY Patient-specific titanium maxillofacial mesh implant
K232889 · Meticuly Co., Ltd. · Apr 2024