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Chattanooga 2876

by Djo, LLC

Chattanooga 2876 is a Class II device made by Djo, LLC, listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00888912297110), 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 Number00888912297110 UDI-DI Date15 Sep 2016ListedStatusListed 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  • Withdrawn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
Chattanooga
Generic name
Multi-modality physical therapy system, simultaneous, professional-use
Model / reference
2876
Primary DI / UDI-DI
00888912297110
FDA product code
IPF
GMDN term
Multi-modality physical therapy system, simultaneous, professional-use
Device class
Class II
Regulation number
890.5850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Physical therapy ultrasound/neuromuscular stimulation system

Similar devices

Other devices filed under FDA product code IPF (Stimulator, muscle, powered).

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

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