510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923876Substantially Equivalent

Riskontrol Single Use

Riskontrol, Santa Fe NM / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923876 is the FDA 510(k) clearance record for RISKONTROL SINGLE USE, a class I device, cleared for Riskontrol on under FDA product code ECB (Unit, Syringe, Air And/Or Water). FDA records list one 510(k) clearance for Riskontrol. As of , FDA records show no recalls naming K923876.

Clearance record

Decision date
Received
(245 days to decision)
Product code
ECB Unit, Syringe, Air And/Or Water
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Riskontrol 524 E. Coronado Rd., Santa Fe NM
510(k) summary
Statement
Third party review
No

Clearances, product code ECB

Trailing 12 months

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

FDA records show no clearances under product code ECB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ECB, 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