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Veraviewepocs

by J. Morita U.S.A., Inc

510(k) K073696

Veraviewepocs is a Class II device made by J. Morita U.S.A., Inc, cleared under FDA 510(k) K073696 on 8 Apr 2008, active as of 8 Nov 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 8 Nov 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK073696 Date8 Apr 2008ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
MUH
FDA applicant
J. Morita USA, Inc.
Device class
Class II
Regulation
21 CFR Part 872.1800
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K073696

7 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K073696
UDI-DISize and differences
Veraviewepocs 3D F40 X-550
J.MORITA MFG.CORP.
X-55004548213020416 —On the market
Veraviewepocs 3D F40 X-550
J.MORITA MFG.CORP.
X-55004548213020430 —On the market
Veraviewepocs 3D R100 X-550
J.MORITA MFG.CORP.
X-55004548213020447 —On the market
Veraviewepocs 3D R100 X-550
J.MORITA MFG.CORP.
X-55004548213020423 —On the market
Veraviewepocs X-550
J.MORITA MFG.CORP.
X-55004548213013708 —On the market
Veraviewepocs X-550
J.MORITA MFG.CORP.
X-55004548213026432 —On the market
Veraviewepocs X550
J.MORITA MFG.CORP.
X55004548213020379 —On the market

Similar devices

Other devices filed under FDA product code MUH (System, X-Ray, Extraoral Source, Digital).

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