Medical Device Manufacturer · US , Irvine , CA

J. Morita USA, Inc. - FDA 510(k) Cleared Devices

52 submissions · 52 cleared · Since 1988

Total

Cleared

Denied

J. Morita USA, Inc. has 52 FDA 510(k) cleared dental devices. Based in Irvine, US.

Last cleared in 2022. Active since 1988.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Fish & Richardson, P.C. as regulatory consultant.

FDA 510(k) Regulatory Record - J. Morita USA, Inc.

52 devices

1-12 of 52

ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A

K120377 · GEX

General & Plastic Surgery · 170d

Cleared May 04, 2012

TRI AUTO MINI - ENDODEONTIC TREATMENT MOTORIZED HANDPIECE

MULTIPLE (APEX LOCATOR), MODEL RCM-7

K090925 · LQY

Dental · 235d

Cleared Oct 16, 2009

AIR TORX, MODEL TRA-200, TRA-200-CP3, TRA-200-CP4

K091065 · EFB

Dental · 185d

Cleared Apr 09, 2008

3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH, MODEL MCT-1F8/F17

K073695 · JAK

Radiology · 100d

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J. Morita USA, Inc. - FDA 510(k) Cleared Devices

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