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Chattanooga 48080-R

by Djo, LLC

Chattanooga 48080-R is a medical device (FDA Class I; FDA product code ISA, Massager, therapeutic, electric) made by Djo, LLC, listed in FDA GUDID since 27 Mar 2025 (UDI-DI 00190446887225), 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 Number00190446887225 UDI-DI Date27 Mar 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  • Withdrawn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
Chattanooga
Generic name
Pneumatic orthopaedic extracorporeal shock wave therapy system
Model / reference
48080-R
Primary DI / UDI-DI
00190446887225
FDA product code
ISA
GMDN term
Pneumatic orthopaedic extracorporeal shock wave therapy system
Device class
Class I
Regulation number
890.5660
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 ISA (Massager, therapeutic, electric).

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)