510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834392Substantially Equivalent

Labial Cuspid Tube

Alexotek Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834392 is the FDA 510(k) clearance record for LABIAL CUSPID TUBE, a class I device, cleared for Alexotek Co. on under FDA product code DZD (Tube, Orthodontic). FDA records list 4 510(k) clearances for Alexotek Co., from to . As of , FDA records show no recalls naming K834392.

Clearance record

Decision date
Received
(76 days to decision)
Product code
DZD Tube, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Applicant
Alexotek Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DZD

Trailing 12 months

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

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