Todd Industries, Inc.: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Todd Industries, Inc.” (first 1981, latest 1981), across 8 product codes in 1 review panel. Median 510(k) review time under this name: 35 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| BYX | Tubing, Pressure And Accessories | 3 | 3 |
| BYF | Mask, Oxygen, Low Concentration, Venturi | 2 | 2 |
| BXJ | Clip, Nose | 1 | 1 |
| BYG | Mask, Oxygen | 1 | 1 |
| BZA | Connector, Airway (Extension) | 1 | 1 |
| BZO | Set, Tubing And Support, Ventilator (W Harness) | 1 | 1 |
| CAT | Cannula, Nasal, Oxygen | 1 | 1 |
| CCQ | Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | 1 | 1 |
Review panels
- Anesthesiology (11)
Most recent Todd Industries, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K810373 | VENTURI MASK/DELIVERY SYSTEM #'S | BYF | 1981-03-17 | 33 |
| K810362 | CORRUGATED FLEX TUBING | BYX | 1981-03-17 | 34 |
| K810361 | CONNECTOR ADAPTERS | BZA | 1981-03-17 | 34 |
| K810344 | OXYGEN TUBING | BYX | 1981-03-17 | 35 |
| K810343 | NEBULIZERS | CCQ | 1981-03-17 | 35 |
| K810342 | NASAL CANNULA | CAT | 1981-03-17 | 35 |
| K810341 | LIFELINE IPPB SET-UP | BZO | 1981-03-17 | 35 |
| K810340 | ADULT MASKS & PEDIATRIC MASKS | BYG | 1981-03-17 | 35 |
| K810339 | NOSECLIP #6118 | BXJ | 1981-03-17 | 36 |
| K810430 | VENTURI MASK/DELIVERY SYSTEM #6078 | BYF | 1981-03-13 | 22 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Todd Industries, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Todd Medical, Inc. (6 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Todd Industries, Inc.?
FDA lists 11 510(k) clearances under the applicant name “Todd Industries, Inc.” (first 1981, latest 1981), across 8 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Todd Industries, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Todd Industries, Inc. is 35 days.
Which FDA product codes appear under Todd Industries, Inc.?
The most frequent FDA product codes under this applicant name are BYX (Tubing, Pressure And Accessories, 3); BYF (Mask, Oxygen, Low Concentration, Venturi, 2); BXJ (Clip, Nose, 1).
Next steps
- See all 11 Todd Industries, Inc. clearances with predicates and recalls
- Run predicate analysis for product code BYX, Todd Industries, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.