Skip to content

Laser Mixture 1

by Red Ball Oxygen Company

Laser Mixture 1 is a Class I device made by Red Ball Oxygen Company, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00860009625907), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860009625907 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Laser Mixture
Generic name
Laser-generating gas
Model / reference
1
Primary DI / UDI-DI
00860009625907
FDA product code
NXF
GMDN term
Laser-generating gas
Device class
Class I
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laser-generating gas

Other devices from Red Ball Oxygen Company

Properties

  • Single use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)