Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Indiba S. A. U. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K241107 | Indiba Diathermia Radiofrequency Deep Care Device (Deep care | Indiba S. A. U. | 2025-01-24 | 277 | 0 |
| K243139 | Reverso Pro System | Indiba S. A. U. | 2025-01-22 | 114 | 0 |
| K243164 | INDIBA COMPACT devices | Indiba S. A. U. | 2024-11-20 | 51 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda