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RT300-LA supine

by Restorative Therapies, Inc.

RT300-LA supine is a Class II device made by Restorative Therapies, Inc., listed in FDA GUDID since 16 Sep 2016 (UDI-DI FA217791), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberFA217791 UDI-DI Date16 Sep 2016ListedStatusListed 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  • Withdrawn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
RT300
Generic name
Physical therapy transcutaneous electrical stimulation system, line-powered
Model / reference
RT300-LA supine
Primary DI / UDI-DI
FA217791
FDA product code
GZI
GMDN term
Physical therapy transcutaneous electrical stimulation system, line-powered
Device class
Class II
Regulation number
882.5810
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GZI (Stimulator, Neuromuscular, External Functional).

Other devices from Restorative Therapies, Inc.

See all devices from Restorative Therapies, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)