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Corix 70 Corix 70 Plus USV

by Coramex, S.A.

Corix 70 Corix 70 Plus USV is a Class II device made by Coramex, S.A., cleared under FDA 510(k) K031802 on 21 Jul 2003 and listed in FDA GUDID since 10 Jan 2024 (UDI-DI 00860010674406), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K031802

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860010674406 UDI-DI Date10 Jan 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK031802 Date21 Jul 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K031802 decided 21 Jul 2003 Active
  • FDA GUDID UDI-DI 00860010674406 listed 10 Jan 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K031802
  2. Listed FDA GUDID 00860010674406

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Corix 70
Generic name
Stationary extraoral dental x-ray system, analogue
Model / reference
Corix 70 Plus USV
Primary DI / UDI-DI
00860010674406
510(k) Number
FDA product code
EHD
GMDN term
Stationary extraoral dental x-ray system, analogue
Device class
Class II
Regulation number
872.1800
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from Coramex, S.A.

Properties

  • Over-the-counter
  • Serial number
Other properties (13, all answered No)