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LIGHTWAVE ReactPRO

by MedAesthetics International LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 NumberG866REACTPRO0 UDI-DI Date8 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Lightwave
Generic Name
Blue/red/infrared phototherapy lamp
Model / Ref / Catalog
ReactPRO, React_PRO
Primary DI / UDI-DI
G866REACTPRO0
510(k) Number
FDA Product Code
GEX
GMDN Term
Blue/red/infrared phototherapy lamp
Device Class
Class II
Regulation Number
878.4810
GUDID distribution status
In Commercial Distribution
Size
Area/Surface Area — 648 Square centimeter

Related devices

Cleared under the same submission (K082586)

Other devices from MedAesthetics International LLC

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No