Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Techstyles — 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) |
|---|---|---|---|---|---|
| K992436 | GOWN BACK, MODEL 13-403N; 13-404N; 13-405N | Techstyles | 2000-01-20 | 182 | 0 |
| K920045 | DURATECH HOSPITAL TOWEL | Techstyles | 1992-07-02 | 178 | 0 |
| K920153 | THERMUFF BAG | Techstyles | 1992-07-01 | 170 | 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