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LZR7 Pro3M

by Lzr7, Inc.

LZR7 Pro3M is a musculoskeletal/physical therapy laser (FDA Class II; FDA product code ILY, Lamp, Infrared, Therapeutic Heating) made by Lzr7, Inc., listed in FDA GUDID since 17 Sep 2019 (UDI-DI B657002), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB657002 UDI-DI Date17 Sep 2019ListedStatusListed 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  • Withdrawn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
LZR7
Generic name
Musculoskeletal/physical therapy laser, home-use
Model / reference
Pro3M
Primary DI / UDI-DI
B657002
FDA product code
ILY
GMDN term
Musculoskeletal/physical therapy laser, home-use
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from Lzr7, Inc.

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)