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Chattanooga 19365

by Djo, LLC

Chattanooga 19365 is a medical device (FDA Class II; FDA product code GZI, Stimulator, Neuromuscular, External Functional) made by Djo, LLC, listed in FDA GUDID since 18 Feb 2022 (UDI-DI 00190446650973), 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 Number00190446650973 UDI-DI Date18 Feb 2022ListedStatusListed 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  • Withdrawn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
Pneumatic orthopaedic extracorporeal shock wave therapy system
Model / reference
19365
Primary DI / UDI-DI
00190446650973
FDA product code
GZI
GMDN term
Pneumatic orthopaedic extracorporeal shock wave therapy system
Device class
Class II
Regulation number
882.5810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pneumatic orthopaedic extracorporeal shock wave therapy system

Similar devices

Other devices filed under FDA product code GZI (STIMULATOR, NEUROMUSCULAR, EXTERNAL FUNCTIONAL).

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)