510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K910465Substantially Equivalent

Meliodent, Denture Resin

Kulzer GmbH, South Bend IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910465 is the FDA 510(k) clearance record for MELIODENT, DENTURE RESIN, a class II device, cleared for Heraeus Kulzer, Inc. on under FDA product code EBI (Resin, Denture, Relining, Repairing, Rebasing). FDA records list 205 510(k) clearances for KULZER GMBH, from to . As of , FDA records show no recalls naming K910465.

Clearance record

Decision date
Received
(122 days to decision)
Product code
EBI Resin, Denture, Relining, Repairing, Rebasing
Regulation
21 CFR 872.3760
Device class
Class II
Review panel
Dental
Applicant
Heraeus Kulzer, Inc. 4315 S Lafayette Blvd., South Bend IN
Third party review
No

Clearances, product code EBI

Trailing 12 months
7 clearances under product code EBI in the twelve months to November 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EBI, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20263
August 20262
September 20260
October 20260
November 20260