Radmedix, LLC: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Radmedix, LLC” (first 2020, latest 2023), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 30 days. Since 2017 the median was 30 days, against 50 days for all cleared 510(k)s in the same product codes. 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 |
|---|---|---|
| 2020 | 3 | 24 |
| 2021 | 1 | 32 |
| 2022 | 0 | — |
| 2023 | 2 | 71 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Radmedix, LLC took a median 30 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 50 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) | 3 | 3 |
| KPR | System, X-Ray, Stationary | 2 | 2 |
| IZL | System, X-Ray, Mobile | 1 | 1 |
Review panels
- Radiology (6)
Most recent Radmedix, LLC 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K231995 | AcuityUDR | KPR | 2023-10-25 | 112 |
| K231709 | AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4 | MQB | 2023-07-12 | 30 |
| K210919 | AcuityDRe | MQB | 2021-04-30 | 32 |
| K201058 | Accuvue+ | MQB | 2020-05-06 | 15 |
| K200726 | AcuityPDR | IZL | 2020-04-13 | 24 |
| K193360 | Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard | KPR | 2020-01-02 | 29 |
Recalls
openFDA lists no recalls under a recalling firm named Radmedix, LLC.
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 Radmedix, LLC?
FDA lists 6 510(k) clearances under the applicant name “Radmedix, LLC” (first 2020, latest 2023), 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 Radmedix, LLC?
The median time from FDA receipt to decision across 510(k)s cleared under the name Radmedix, LLC is 30 days. Since 2017: 30 days, versus 50 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Radmedix, LLC?
The most frequent FDA product codes under this applicant name are MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager), 3); KPR (System, X-Ray, Stationary, 2); IZL (System, X-Ray, Mobile, 1).
Next steps
- See all 6 Radmedix, LLC clearances with predicates and recalls
- Run predicate analysis for product code MQB, Radmedix, LLC'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.