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AirTouch AirTouch 905

by Livermoretech, 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 Number00860015089205 UDI-DI Date3 Sep 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  • Withdrawn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
AirTouch
Generic Name
Portable basic diagnostic x-ray system, digital
Model / Reference
AirTouch 905
Primary DI / UDI-DI
00860015089205
510(k) Number
FDA Product Code
IZL
GMDN Term
Portable basic diagnostic x-ray system, digital
Device Class
Class II
Regulation Number
892.1720
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K244049)

Other devices from Livermoretech, Inc

See all devices from Livermoretech, Inc →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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