510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895064Substantially Equivalent

Monogram II

Leach and Dillon Co., Inc., Mansfield MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895064 is the FDA 510(k) clearance record for MONOGRAM II, a class II device, cleared for Leach and Dillon Co., Inc. on under FDA product code EJT (Alloy, Gold-Based Noble Metal). FDA records list 31 510(k) clearances for Leach and Dillon Co., Inc., from to . As of , FDA records show no recalls naming K895064.

Clearance record

Decision date
Received
(132 days to decision)
Product code
EJT Alloy, Gold-Based Noble Metal
Regulation
21 CFR 872.3060
Device class
Class II
Review panel
Dental
Applicant
Leach and Dillon Co., Inc. 171 Forbes Blvd., Mansfield MA
Third party review
No

Clearances, product code EJT

Trailing 12 months

FDA records hold no clearances under product code EJT in the trailing twelve months.

FDA records show no clearances under product code EJT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EJT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260