Cleared Traditional

K260137 - KLS Martin IPS Oral-Max Implants - MR Conditional

Also marketed or referenced as:
Individual Patient Solutions - Ti (IPS-Ti) Individual Patient Solutions - PEEK (IPS-PEEK) KLS Martin Individual Patient Solutions

K260137 is an FDA 510(k) clearance for KLS Martin IPS Oral-Max Implants - MR C..., manufactured by KLS-Martin L.P.. The device is a Class 2 Dental device with product code JEY cleared through the Traditional 510(k) pathway after a 213-day FDA review.

K260137 · KLS-Martin L.P. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2026
Decision
213d
Days
Class 2
Risk

K260137 is an FDA 510(k) clearance for the KLS Martin IPS Oral-Max Implants - MR Conditional. 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 17, 2026 after a review of 213 days - an extended review cycle.

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

FDA 510(k) Submission Details - K260137

510(k) Number K260137 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 2026
Decision Date August 17, 2026
Days to Decision 213 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
86d slower than avg
Panel avg: 127d · This submission: 213d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JEY Device Classification - Class 2, Special Controls

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 249
Devices cleared under the same product code (JEY) and FDA review panel - the closest regulatory comparables to K260137.
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KLS Martin Oral-Max Implants MR Conditional (bundled)
K241314 · KLS-Martin L.P. · Aug 2024
MRI Universal
K240651 · Stryker Leibinger GmbH & Co KG · Jul 2024