Siemens Medical Solutions USA, Inc., Ultrasound DI: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Siemens Medical Solutions USA, Inc., Ultrasound DI” (first 2007, latest 2017), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 44 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Caduvo groups this applicant name under Siemens Healthineers, based on public ownership records.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 1 | 79 |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 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 Siemens Medical Solutions USA, Inc., Ultrasound DI took a median 79 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 109 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| IYN | System, Imaging, Pulsed Doppler, Ultrasonic | 8 | 8 |
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | 2 | 2 |
| JAK | System, X-Ray, Tomography, Computed | 1 | 1 |
Review panels
- Radiology (11)
Most recent Siemens Medical Solutions USA, Inc., Ultrasound DI 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K163289 | syngo. CT Single Source Dual Energy (twin beam) | JAK | 2017-02-09 | 79 |
| K113179 | ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM | IYN | 2011-12-07 | 40 |
| K112596 | ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM | IYN | 2011-09-16 | 9 |
| K081148 | SIEMENS ACUSON 2000 ULTRASOUND SYSTEM WITH ABVS TRANSDUCER | IYO | 2008-12-22 | 244 |
| K082142 | ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM | IYN | 2008-11-13 | 106 |
| K081121 | MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM | IYO | 2008-06-04 | 44 |
| K080760 | ACUSON X300 ULTRASOUND SYSTEM | IYN | 2008-04-25 | 38 |
| K072365 | SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM | IYN | 2007-10-17 | 55 |
| K072090 | SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMS | IYN | 2007-09-14 | 46 |
| K071036 | MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM | IYN | 2007-05-16 | 34 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Siemens Medical Solutions USA, Inc., Ultrasound DI.
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.
- Siemens Medical Solutions USA, Inc. (784 510(k)s)
- Siemens Healthcare Diagnostics, Inc. (245 510(k)s)
- Siemens Corp. (67 510(k)s)
- Siemens Elema AB (63 510(k)s)
- Siemens Gammasonics, Inc. (53 510(k)s)
- Siemens Hearing Instruments, Inc. (42 510(k)s)
- Siemens Healthcare GmbH (32 510(k)s)
- Siemens Medi Cal Solutions, Inc. (32 510(k)s)
- Siemens AG Medical Solutions (31 510(k)s)
- Siemens Medical Systems, Inc. (25 510(k)s)
- Siemens Healthcare Diagnostics Products GmbH (23 510(k)s)
- Siemens AG (15 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Siemens Medical Solutions USA, Inc., Ultrasound DI?
FDA lists 11 510(k) clearances under the applicant name “Siemens Medical Solutions USA, Inc., Ultrasound DI” (first 2007, latest 2017), 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 Siemens Medical Solutions USA, Inc., Ultrasound DI?
The median time from FDA receipt to decision across 510(k)s cleared under the name Siemens Medical Solutions USA, Inc., Ultrasound DI is 44 days.
Which FDA product codes appear under Siemens Medical Solutions USA, Inc., Ultrasound DI?
The most frequent FDA product codes under this applicant name are IYN (System, Imaging, Pulsed Doppler, Ultrasonic, 8); IYO (System, Imaging, Pulsed Echo, Ultrasonic, 2); JAK (System, X-Ray, Tomography, Computed, 1).
Next steps
- See all 11 Siemens Medical Solutions USA, Inc., Ultrasound DI clearances with predicates and recalls
- Run predicate analysis for product code IYN, Siemens Medical Solutions USA, Inc., Ultrasound DI'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.