510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K810869Substantially Equivalent

Silicone Elastomer Kit

Rapid Injection Systems Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810869 is the FDA 510(k) clearance record for SILICONE ELASTOMER KIT, a class II device, cleared for Rapid Injection Systems Corp. on under FDA product code EBI (Resin, Denture, Relining, Repairing, Rebasing). FDA records list 2 510(k) clearances for Rapid Injection Systems Corp., from to . As of , FDA records show no recalls naming K810869.

Clearance record

Decision date
Received
(29 days to decision)
Product code
EBI Resin, Denture, Relining, Repairing, Rebasing
Regulation
21 CFR 872.3760
Device class
Class II
Review panel
Dental
Applicant
Rapid Injection Systems Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EBI

Trailing 12 months
10 clearances under product code EBI in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EBI, trailing twelve months
MonthClearances
November 20253
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20263
August 20262
September 20260
October 20260