Sentec AG: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Sentec AG” (first 2007, latest 2025), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 213 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 | 1 | 213 |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 1 | 273 |
| 2025 | 1 | 244 |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Sentec AG took a median 258 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 214 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LKD | Monitor, Carbon-Dioxide, Cutaneous | 3 | 3 |
| DQA | Oximeter | 1 | 1 |
| QEB | Ventilatory Electrical Impedance Tomograph | 1 | 1 |
Review panels
- Anesthesiology (5)
Most recent Sentec AG 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K243765 | LuMon(TM) System | QEB | 2025-08-07 | 244 |
| K232516 | Sentec Digital Monitoring System (SDMS) tCOM+ | LKD | 2024-05-17 | 273 |
| K151329 | SenTec Digital Monitor, OxiVenT Sensor, V-Sign Sensor, Staysite Adhesive Pad, V-STATS PC Software including V-CareNet | LKD | 2015-12-17 | 213 |
| K101690 | SENTEC DIGITAL MONITOR, V-SIGN SENSOR AND V-SIGN SENSOR 2 WITH DIGITAL SENSOR ADAPER CABLE | LKD | 2010-12-03 | 170 |
| K071672 | SENTEC DIGITAL MONITORING SYSTEM | DQA | 2007-09-12 | 85 |
Recalls
14 product recalls in 9 recall events; 3 initiated in the last five years. Most recent: 2023-07-25.
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.
- Sentec, Inc. (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Sentec AG?
FDA lists 5 510(k) clearances under the applicant name “Sentec AG” (first 2007, latest 2025), 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 Sentec AG?
The median time from FDA receipt to decision across 510(k)s cleared under the name Sentec AG is 213 days.
Which FDA product codes appear under Sentec AG?
The most frequent FDA product codes under this applicant name are LKD (Monitor, Carbon-Dioxide, Cutaneous, 3); DQA (Oximeter, 1); QEB (Ventilatory Electrical Impedance Tomograph, 1).
Next steps
- See all 5 Sentec AG clearances with predicates and recalls
- Run predicate analysis for product code LKD, Sentec AG'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.