Skip to content

Vaporox 30-0006

by Vaporox, 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 Number00850038157067 UDI-DI Date11 Aug 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  • Withdrawn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
Vaporox
Generic Name
Extremity-oxygenation hyperbaric chamber, powered
Model / Reference
30-0006
Primary DI / UDI-DI
00850038157067
510(k) Number
FDA Product Code
KPJ
GMDN Term
Extremity-oxygenation hyperbaric chamber, powered
Device Class
Class II
Regulation Number
878.5650
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250188)

Other devices from Vaporox, Inc.

See all devices from Vaporox, Inc. →

Properties

  • Prescription Use
  • Lot / Batch 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
  • Serial Number: No
  • Expiration Date: No