Skip to content

Regenesis 3 1

by Ochs Labs LLC

Regenesis 3 1 is a Class II device made by Ochs Labs LLC, listed in FDA GUDID since 4 Feb 2025 (UDI-DI G253R30), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG253R30 UDI-DI Date4 Feb 2025ListedStatusListed 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  • Withdrawn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
Regenesis 3
Generic name
Red/infrared light phototherapy unit
Model / reference
1
Primary DI / UDI-DI
G253R30
FDA product code
ILY
GMDN term
Red/infrared light phototherapy unit
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Red/infrared light phototherapy unit

Similar devices

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

Other devices from Ochs Labs LLC

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)