Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Todd Industries, Inc. — Predicate Candidate Screening
11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
35 daysmedian FDA review time
35 days90th percentile
11clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K810373 | VENTURI MASK/DELIVERY SYSTEM #'S | Todd Industries, Inc. | 1981-03-17 | 33 | 0 |
| K810361 | CONNECTOR ADAPTERS | Todd Industries, Inc. | 1981-03-17 | 34 | 0 |
| K810342 | NASAL CANNULA | Todd Industries, Inc. | 1981-03-17 | 35 | 0 |
| K810344 | OXYGEN TUBING | Todd Industries, Inc. | 1981-03-17 | 35 | 0 |
| K810343 | NEBULIZERS | Todd Industries, Inc. | 1981-03-17 | 35 | 0 |
| K810341 | LIFELINE IPPB SET-UP | Todd Industries, Inc. | 1981-03-17 | 35 | 0 |
| K810362 | CORRUGATED FLEX TUBING | Todd Industries, Inc. | 1981-03-17 | 34 | 0 |
| K810340 | ADULT MASKS & PEDIATRIC MASKS | Todd Industries, Inc. | 1981-03-17 | 35 | 0 |
| K810339 | NOSECLIP #6118 | Todd Industries, Inc. | 1981-03-17 | 36 | 0 |
| K810430 | VENTURI MASK/DELIVERY SYSTEM #6078 | Todd Industries, Inc. | 1981-03-13 | 22 | 0 |
| K810374 | CORRUGATED FLEX TUBING #6000, | Todd Industries, Inc. | 1981-03-13 | 29 | 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