Skip to content

Renpho SM9075

by Joicom Corporation

Renpho SM9075 is a medical device (FDA Class II) made by Joicom Corporation, listed in FDA GUDID since 20 Oct 2025 (UDI-DI 00810140062680), 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 Number00810140062680 UDI-DI Date20 Oct 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  • Withdrawn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
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / reference
SM9075
Primary DI / UDI-DI
00810140062680
FDA product code
NUH, NGX, IPF, GZJ
GMDN term
Physical therapy transcutaneous neuromuscular electrical stimulation system
Device class
Class II
Regulation number
882.5890, 890.5850
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter).

Other devices from Joicom Corporation

See all devices from Joicom Corporation →

Properties

  • Serial number
Other properties (14, all answered No)