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Diowave Stealth Max DSM

by Technological Medical Advancements L.L.C.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG180DIOWAVESTEALTHMAX0 UDI-DI Date12 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Diowave
Generic Name
Musculoskeletal infrared phototherapy unit, non-wearable
Model / Reference
Diowave Stealth Max DSM
Primary DI / UDI-DI
G180DIOWAVESTEALTHMAX0
FDA Product Code
ILY
GMDN Term
Musculoskeletal infrared phototherapy unit, non-wearable
Device Class
Class II
Regulation Number
890.5500
GUDID distribution status
In Commercial Distribution

Other devices from Technological Medical Advancements L.L.C.

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No