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ScanX Duo Touch J1205E

by Air Techniques, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD678J1205E0 UDI-DI Date27 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ScanX Duo Touch
Generic Name
Dental computed radiography digital imaging scanner
Model / Ref / Catalog
J1205E, J1200E
Primary DI / UDI-DI
D678J1205E0
510(k) Number
FDA Product Code
MUH
GMDN Term
Dental computed radiography digital imaging scanner
Device Class
Class II
Regulation Number
872.1800
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K191623)

Other devices from Air Techniques, Inc.

See all devices from Air Techniques, Inc. →

Properties

  • Serial Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No