Etiometry, Inc.: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Etiometry, Inc.” (first 2015, latest 2026), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 219 days. Since 2017 the median was 242 days, against 217 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 |
|---|---|---|
| 2015 | 2 | 144 |
| 2016 | 1 | 233 |
| 2017 | 1 | 205 |
| 2018 | 0 | — |
| 2019 | 1 | 303 |
| 2020 | 1 | 103 |
| 2021 | 0 | — |
| 2022 | 1 | 266 |
| 2023 | 2 | 331 |
| 2024 | 0 | — |
| 2025 | 1 | 264 |
| 2026 | 1 | 106 |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Etiometry, Inc. took a median 242 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 217 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | 5 | 5 |
| PPW | Adjunctive Cardiovascular Status Indicator | 4 | 4 |
| PLB | Multivariate Vital Signs Index | 2 | 2 |
Review panels
- Cardiovascular (11)
Most recent Etiometry, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K254066 | Etiometry Platform | PPW | 2026-04-03 | 106 |
| K241479 | Etiometry Platform (DAV 5.4 RAE 9.2) | PPW | 2025-02-12 | 264 |
| K223578 | T3 Platform software | PPW | 2023-07-07 | 219 |
| K213423 | T3 Platform software | PLB | 2023-01-06 | 443 |
| K213230 | T3 Platform Software | PPW | 2022-06-22 | 266 |
| K202306 | T3 Platform software | MWI | 2020-11-25 | 103 |
| K190273 | T3 Platform software | MWI | 2019-12-08 | 303 |
| K163065 | T3 Software | MWI | 2017-05-26 | 205 |
| K152258 | T3 Software | PLB | 2016-03-31 | 233 |
| K151715 | T3 Software | MWI | 2015-10-29 | 126 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Etiometry, Inc..
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 Etiometry, Inc.?
FDA lists 11 510(k) clearances under the applicant name “Etiometry, Inc.” (first 2015, latest 2026), 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 Etiometry, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Etiometry, Inc. is 219 days. Since 2017: 242 days, versus 217 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Etiometry, Inc.?
The most frequent FDA product codes under this applicant name are MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms), 5); PPW (Adjunctive Cardiovascular Status Indicator, 4); PLB (Multivariate Vital Signs Index, 2).
Next steps
- See all 11 Etiometry, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MWI, Etiometry, Inc.'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.