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Chattanooga 2738-2

by Djo, LLC

Chattanooga 2738-2 is a Class II device made by Djo, LLC, listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00888912292160), 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 Number00888912292160 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  • Withdrawn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
Physical therapy ultrasound system
Model / reference
2738-2
Primary DI / UDI-DI
00888912292160
FDA product code
IMG
GMDN term
Physical therapy ultrasound system
Device class
Class II
Regulation number
890.5860
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IMG (STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT).

Other devices from Djo, LLC

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Properties

  • Contains latex
  • Prescription use
  • Manufacturing date
Other properties (12, all answered No)