510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K040891Substantially Equivalent

Kls Martin Ortho Anchorage System (Plates)

KLS-Martin L.P., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K040891 is the FDA 510(k) clearance record for KLS MARTIN ORTHO ANCHORAGE SYSTEM (PLATES), a class II device, cleared for KLS-Martin L.P. on under FDA product code DZE (Implant, Endosseous, Root-Form). FDA records list 78 510(k) clearances for KLS-Martin L.P., from to . As of , FDA records show no recalls naming K040891.

Clearance record

Decision date
Received
(53 days to decision)
Product code
DZE Implant, Endosseous, Root-Form
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
KLS-Martin L.P. 11239-1 St. John'S Ind. Pkwy., Jacksonville FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DZE

Trailing 12 months
19 clearances under product code DZE in the twelve months to November 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code DZE, trailing twelve months
MonthClearances
December 20254
January 20261
February 20262
March 20264
April 20260
May 20261
June 20264
July 20260
August 20261
September 20261
October 20261
November 20260