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Laspot Gd-P-E

by Wuhan Guangdun Technology Co., Ltd..

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 Number06957510600852 UDI-DI Date23 Sep 2025ListedStatusListed 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  • Withdrawn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
Laspot
Generic Name
Musculoskeletal/physical therapy laser, home-use
Model / Reference
GD-P-E
Primary DI / UDI-DI
06957510600852
510(k) Number
FDA Product Code
NHN
GMDN Term
Musculoskeletal/physical therapy laser, home-use
Device Class
Class II
Regulation Number
890.5500
GUDID distribution status
In Commercial Distribution

Other devices from Wuhan Guangdun Technology Co., Ltd..

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

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