510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992648Substantially Equivalent

Rotary Master

J. Morita USA, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992648 is the FDA 510(k) clearance record for ROTARY MASTER, a class I device, cleared for J. Morita USA, Inc. on under FDA product code EBW (Controller, Foot, Handpiece And Cord). FDA records list 52 510(k) clearances for J. Morita USA, Inc., from to . As of , FDA records show no recalls naming K992648.

Clearance record

Decision date
Received
(178 days to decision)
Product code
EBW Controller, Foot, Handpiece And Cord
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
J. Morita USA, Inc. 601 13th St. NW, Washington DC
510(k) summary
Statement
Third party review
No

Clearances, product code EBW

Trailing 12 months
2 clearances under product code EBW in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EBW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260