Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Innovative Therapies, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K111333 | ANTLIA III WOUND TREATMENT SYSTEM | Innovative Therapies, Inc. | 2011-08-08 | 88 | 0 |
| K093564 | SVED WOUND TREATMENT SYSTEM | Innovative Therapies, Inc. | 2009-11-25 | 7 | 0 |
| K071301 | ANTLIA I WOUND IRRIGATION SYSTEM | Innovative Therapies, Inc. | 2007-05-24 | 15 | 0 |
| K070904 | ANTLIA II SUCTION PUMP SYSTEM | Innovative Therapies, Inc. | 2007-04-13 | 11 | 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