Trident S.R.L: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Trident S.R.L” (first 2016, latest 2023), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 36 days. Since 2017 the median was 36 days, against 79 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 |
|---|---|---|
| 2016 | 2 | 36 |
| 2017 | 0 | — |
| 2018 | 1 | 29 |
| 2019 | 0 | — |
| 2020 | 1 | 36 |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 1 | 307 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Trident S.R.L took a median 36 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 79 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MUH | System, X-Ray, Extraoral Source, Digital | 3 | 3 |
| EHD | Unit, X-Ray, Extraoral With Timer | 1 | 1 |
| OAS | X-Ray, Tomography, Computed, Dental | 1 | 1 |
Review panels
- Radiology (5)
Most recent Trident S.R.L 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K222666 | X-View 3D Pan/X-View 2D Pan | OAS | 2023-07-10 | 307 |
| K200625 | I-View Gold and Imagen Gold Dental Sensors | MUH | 2020-04-15 | 36 |
| K182206 | RiX70 DC | EHD | 2018-09-13 | 29 |
| K162619 | I View and Imagen Sensor | MUH | 2016-11-04 | 45 |
| K160386 | ReadeR, VieweR, QuickScan PSP | MUH | 2016-03-10 | 28 |
Recalls
openFDA lists no recalls under a recalling firm named Trident S.R.L.
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.
- Trident Dental, Inc. (3 510(k)s)
- Trident Medical Products, Inc. (3 510(k)s)
- Trident Surgical Corp. (2 510(k)s)
- Trident Orthopedics (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Trident S.R.L?
FDA lists 5 510(k) clearances under the applicant name “Trident S.R.L” (first 2016, 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 Trident S.R.L?
The median time from FDA receipt to decision across 510(k)s cleared under the name Trident S.R.L is 36 days. Since 2017: 36 days, versus 79 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Trident S.R.L?
The most frequent FDA product codes under this applicant name are MUH (System, X-Ray, Extraoral Source, Digital, 3); EHD (Unit, X-Ray, Extraoral With Timer, 1); OAS (X-Ray, Tomography, Computed, Dental, 1).
Next steps
- See all 5 Trident S.R.L clearances with predicates and recalls
- Run predicate analysis for product code MUH, Trident S.R.L'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.