Easyglide , Ltd.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Easyglide , Ltd.” (first 2009, latest 2012), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 172 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 | 2 | 209 |
| 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 |
|---|---|---|---|
| FDF | Colonoscope And Accessories, Flexible/Rigid | 2 | 2 |
| FDS | Gastroscope And Accessories, Flexible/Rigid | 2 | 2 |
| ODC | Endoscope Channel Accessory | 1 | 1 |
Review panels
Most recent Easyglide , Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K113166 | CLEARPATH UPPER GI | FDS | 2012-05-16 | 202 |
| K113050 | CLEARPATH LOWER GI | FDF | 2012-05-16 | 216 |
| K101094 | CLEARJET | ODC | 2010-05-17 | 27 |
| K093779 | CLEARPATH UGI | FDS | 2010-03-09 | 90 |
| K091305 | CLEARPATH | FDF | 2009-10-23 | 172 |
Recalls
openFDA lists no recalls under a recalling firm named Easyglide , Ltd..
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 Easyglide , Ltd.?
FDA lists 5 510(k) clearances under the applicant name “Easyglide , Ltd.” (first 2009, latest 2012), across 3 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 Easyglide , Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Easyglide , Ltd. is 172 days.
Which FDA product codes appear under Easyglide , Ltd.?
The most frequent FDA product codes under this applicant name are FDF (Colonoscope And Accessories, Flexible/Rigid, 2); FDS (Gastroscope And Accessories, Flexible/Rigid, 2); ODC (Endoscope Channel Accessory, 1).
Next steps
- See all 5 Easyglide , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code FDF, Easyglide , 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 (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.