510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923462Substantially Equivalent

Delight

Planmeca U.S.A. Inc, Finland, FI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923462 is the FDA 510(k) clearance record for DELIGHT, a class I device, cleared for Planmeca USA, Inc. on under FDA product code EAZ (Light, Operating, Dental). FDA records list 13 510(k) clearances for Planmeca USA, Inc., from to . As of , FDA records show no recalls naming K923462.

Clearance record

Decision date
Received
(160 days to decision)
Product code
EAZ Light, Operating, Dental
Regulation
21 CFR 872.4630
Device class
Class I
Review panel
Dental
Applicant
Planmeca USA, Inc. Asentajasnkatu 6, Finland, FI
510(k) summary
Statement
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