FDA applicant
Chattanooga Group, Inc.
FDA records 81 decisions for Chattanooga Group, Inc. (Hixson, TN) from 1980 to 2009: 81 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMG (Stimulator, Ultrasound And Muscle, For Use In…). Its devices cite 23 predicates, 3 of them its own earlier devices. 22 recalls are linked to its devices.
FDA’s records also spell it “Chattanooga Group”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Chattanooga Group, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
3in 2009
2026 so far, outlined.
Recalls per year
1in 2015
Class I Class II/III not classified
Planning a device like Chattanooga Group, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Chattanooga”
FDA records each applicant name separately; these may or may not be the same firm.