510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020080Substantially Equivalent

Bonart Art-E1 Electrosurgery Unit

Diagnostic Data, Inc., Upland CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K020080 is the FDA 510(k) clearance record for BONART ART-E1 ELECTROSURGERY UNIT, a class II device, cleared for Diagnostic Data, Inc. on under FDA product code EKZ (Unit, Electrosurgical, And Accessories, Dental). FDA records list one 510(k) clearance for Diagnostic Data, Inc. As of , FDA records show no recalls naming K020080.

Clearance record

Decision date
Received
(41 days to decision)
Product code
EKZ Unit, Electrosurgical, And Accessories, Dental
Regulation
21 CFR 872.4920
Device class
Class II
Review panel
Dental
Applicant
Diagnostic Data, Inc. 1342-D N. Benson Ave., Upland CA
510(k) summary
Statement
Third party review
No

Clearances, product code EKZ

Trailing 12 months

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

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