510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K861681Substantially Equivalent

Dentimedic Dental Emergency Kit

Dentimedic, Pocomoke City MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861681 is the FDA 510(k) clearance record for DENTIMEDIC DENTAL EMERGENCY KIT, a class I device, cleared for Dentimedic on under FDA product code EMB (Zinc Oxide Eugenol). FDA records list one 510(k) clearance for Dentimedic. As of , FDA records show no recalls naming K861681.

Clearance record

Decision date
Received
(145 days to decision)
Product code
EMB Zinc Oxide Eugenol
Regulation
21 CFR 872.3275
Device class
Class I
Review panel
Dental
Applicant
Dentimedic 102 Eighth St., Pocomoke City MD
Third party review
No

Clearances, product code EMB

Trailing 12 months

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

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