510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902894Substantially Equivalent

Post Cement (Dental Composite)

Medical Device Inspection Company, Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902894 is the FDA 510(k) clearance record for POST CEMENT (DENTAL COMPOSITE), a class II device, cleared for Medical Device Inspection Co., Inc. on under FDA product code EMA (Cement, Dental). FDA records list 30 510(k) clearances for Medical Device Inspection Co., Inc., from to . As of , FDA records show no recalls naming K902894.

Clearance record

Decision date
Received
(30 days to decision)
Product code
EMA Cement, Dental
Regulation
21 CFR 872.3275
Device class
Class II
Review panel
Dental
Applicant
Medical Device Inspection Co., Inc. 55 Northern Blvd., Suite 301, Great Neck NY
Third party review
No

Clearances, product code EMA

Trailing 12 months
10 clearances under product code EMA in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EMA, trailing twelve months
MonthClearances
November 20250
December 20253
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20261
August 20262
September 20261
October 20260