510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902685Substantially Equivalent

Defiance Model Fus 336

Defiance Electronics, Inc., Lenoir City TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902685 is the FDA 510(k) clearance record for DEFIANCE MODEL FUS 336, a class I device, cleared for Defiance Electronics, Inc. on under FDA product code EAZ (Light, Operating, Dental). FDA records list 2 510(k) clearances for Defiance Electronics, Inc., from to . As of , FDA records show no recalls naming K902685.

Clearance record

Decision date
Received
(90 days to decision)
Product code
EAZ Light, Operating, Dental
Regulation
21 CFR 872.4630
Device class
Class I
Review panel
Dental
Applicant
Defiance Electronics, Inc. Rte. 4 Box 167, Hwy. 11, Lenoir City TN
Third party review
No

Clearances, product code EAZ

Trailing 12 months

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

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