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Corix 70 Plus-Usv

by Coramex, S.A.

510(k) K031802

Corix 70 Plus-Usv is a Class II device made by Coramex, S.A., cleared under FDA 510(k) K031802 on 21 Jul 2003, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK031802 Date21 Jul 2003ClearedStatusActive

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  • Withdrawn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
EHD
Device class
Class II
Regulation
21 CFR Part 872.1800
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Devices cleared under K031802

1 device · 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 K031802
UDI-DISize and differences
Corix 70 Corix 70 Plus USV
Coramex, S.A.
Corix 70 Plus USV00860010674406 —On the market

Similar devices

Other devices filed under FDA product code EHD (Unit, X-Ray, Extraoral With Timer).

Other devices from Coramex, S.A.