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SportLaser

by Multi Radiance Medical

SportLaser (800-302) is a Class II device made by Multi Radiance Medical, listed in FDA GUDID since 16 Jan 2025 (UDI-DI 00852556007374), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852556007374 UDI-DI Date16 Jan 2025ListedStatusListed 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  • Withdrawn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

Generic name
Musculoskeletal infrared phototherapy unit, non-wearable
Model / Ref / Catalog
SportLaser, 800-302
Primary DI / UDI-DI
00852556007374
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

Related devices

Category: Musculoskeletal infrared phototherapy unit, non-wearable

Similar devices

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

Other devices from Multi Radiance Medical

See all devices from Multi Radiance Medical →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)