510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934783Substantially Equivalent

Kavo Intrasept 905

Kavo America, Lake Zurich IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934783 is the FDA 510(k) clearance record for KAVO INTRASEPT 905, a class I device, cleared for Kavo America on under FDA product code EIA (Unit, Operative Dental). FDA records list 24 510(k) clearances for Kavo America, from to . As of , FDA records show no recalls naming K934783.

Clearance record

Decision date
Received
(222 days to decision)
Product code
EIA Unit, Operative Dental
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
Kavo America 340 E. Main St., Lake Zurich IL
510(k) summary
Statement
Third party review
No

Clearances, product code EIA

Trailing 12 months
2 clearances under product code EIA in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EIA, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260