Digimed Corporation: FDA filings under this applicant name
FDA lists 2 510(k) clearances under the applicant name “Digimed Corporation” (first 2008, latest 2011), across 1 product code in 1 review panel. Median 510(k) review time under this name: 89 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 |
|---|---|---|---|
| EHD | Unit, X-Ray, Extraoral With Timer | 2 | 2 |
Review panels
- Radiology (2)
Most recent Digimed Corporation 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K103600 | PORTABLE X-RAY SYSTEM | EHD | 2011-04-08 | 121 |
| K082167 | PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX | EHD | 2008-09-26 | 57 |
Recalls
openFDA lists no recalls under a recalling firm named Digimed Corporation.
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.
- Digimed Co., Ltd. (4 510(k)s)
- Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Digimed Corporation?
FDA lists 2 510(k) clearances under the applicant name “Digimed Corporation” (first 2008, latest 2011), across 1 product code 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 Digimed Corporation?
The median time from FDA receipt to decision across 510(k)s cleared under the name Digimed Corporation is 89 days.
Which FDA product codes appear under Digimed Corporation?
The most frequent FDA product codes under this applicant name are EHD (Unit, X-Ray, Extraoral With Timer, 2).
Next steps
- See all 2 Digimed Corporation clearances with predicates and recalls
- Run predicate analysis for product code EHD, Digimed Corporation'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.