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PowerLaser Basic 1200 Cool Grey 35122

by Powermedic ApS

PowerLaser Basic 1200 Cool Grey 35122, a musculoskeletal/physical therapy laser (FDA Class II; FDA product code ILY, Lamp, Infrared, Therapeutic Heating) made by Powermedic ApS, was listed in FDA GUDID on 13 Jun 2023 (UDI-DI 57135920351227); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number57135920351227 UDI-DI Date13 Jun 2023ListedStatusListed GUDID: not 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  • Withdrawn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
PowerLaser Basic 1200 Cool Grey
Generic name
Musculoskeletal/physical therapy laser, home-use
Model / reference
35122
Primary DI / UDI-DI
57135920351227
FDA product code
ILY
GMDN term
Musculoskeletal/physical therapy laser, home-use
Device class
Class II
Regulation number
890.5500
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).

Other devices from Powermedic ApS

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)