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Renpho Rejuven E100B

by Joicom Corporation 2 variants

Renpho Rejuven E100B is a red/blue light phototherapy unit (FDA Class II) made by Joicom Corporation, listed in FDA GUDID since 6 Aug 2025 (UDI-DI 00810140062598), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810140062598 UDI-DI Date6 Aug 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  • Withdrawn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

Trade name
Renpho Rejuven
Generic name
Red/blue light phototherapy unit
Model / reference
E100B
Primary DI / UDI-DI
00810140062598
FDA product code
OLP, OHS
GMDN term
Red/blue light phototherapy unit
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Red/blue light phototherapy unit

Similar devices

Other devices filed under FDA product code OLP (Over-The-Counter Powered Light Based Laser For Acne).

Other devices from Joicom Corporation

See all devices from Joicom Corporation →

Properties

  • Lot / batch number
Other properties (14, all answered No)