510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790078Substantially Equivalent

Bar & Rider, Screws, Tubes

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

K790078 is the FDA 510(k) clearance record for BAR & RIDER, SCREWS, TUBES, a class I device, cleared for Eurodent, Inc. on under FDA product code ECG (Sterilizer, Boiling Water). FDA records list 6 510(k) clearances for Eurodent, Inc., from to . As of , FDA records show no recalls naming K790078.

Clearance record

Decision date
Received
(48 days to decision)
Product code
ECG Sterilizer, Boiling Water
Regulation
21 CFR 872.6710
Device class
Class I
Review panel
Dental
Applicant
Eurodent, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ECG

Trailing 12 months

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

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