Boddingtons Plastics, Ltd.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Boddingtons Plastics, Ltd.” (first 2012, latest 2020), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 42 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 | 1 | 13 |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 1 | 42 |
| 2016 | 1 | 126 |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 1 | 38 |
| 2020 | 1 | 260 |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Boddingtons Plastics, Ltd. took a median 149 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 113 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| FED | Endoscopic Access Overtube, Gastroenterology-Urology | 4 | 4 |
| FDA | Enteroscope And Accessories | 1 | 1 |
Review panels
Most recent Boddingtons Plastics, Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K191330 | Arc Enterocuff | FDA | 2020-01-31 | 260 |
| K191067 | Arc Endocuff Glide AEG110 & AEG120 | FED | 2019-05-30 | 38 |
| K162205 | Arc EndoCuff and Arc EndoCuff Vision | FED | 2016-12-09 | 126 |
| K151801 | Arc Endocuff Vision | FED | 2015-08-13 | 42 |
| K122565 | ARC ENDOCUFF | FED | 2012-09-04 | 13 |
Recalls
1 product recalls in 1 recall events; 0 initiated in the last five years. Most recent: 2020-03-11.
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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Boddingtons Plastics, Ltd.?
FDA lists 5 510(k) clearances under the applicant name “Boddingtons Plastics, Ltd.” (first 2012, latest 2020), across 2 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 Boddingtons Plastics, Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Boddingtons Plastics, Ltd. is 42 days.
Which FDA product codes appear under Boddingtons Plastics, Ltd.?
The most frequent FDA product codes under this applicant name are FED (Endoscopic Access Overtube, Gastroenterology-Urology, 4); FDA (Enteroscope And Accessories, 1).
Next steps
- See all 5 Boddingtons Plastics, Ltd. clearances with predicates and recalls
- Run predicate analysis for product code FED, Boddingtons Plastics, Ltd.'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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.