Hydrofera, LLC: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Hydrofera, LLC” (first 1998, latest 2019), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 119 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 | 1 | 296 |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 1 | 271 |
| 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 Hydrofera, LLC took a median 271 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 232 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| FRO | Dressing, Wound, Drug | 4 | 4 |
| EFQ | Gauze/Sponge, Internal | 1 | 1 |
| EMX | Balloon, Epistaxis | 1 | 1 |
| HOZ | Sponge, Ophthalmic | 1 | 1 |
Review panels
Most recent Hydrofera, LLC 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K190268 | Hydrofera Blue READY - Border | FRO | 2019-11-06 | 271 |
| K130670 | HYDROFERA BLUE PU BACTERIOSTATIC DRESSING | FRO | 2014-01-02 | 296 |
| K023138 | HYDROFERA BACTERIOSTATIC WOUND DRESSING | FRO | 2003-01-17 | 119 |
| K013462 | HYDROFERA BACTERIOSTATIC WOUND DRESSING | FRO | 2002-01-11 | 85 |
| K983276 | HYDROFERA BACTERISTATIC NASAL DRESSING | EMX | 1999-09-14 | 362 |
| K974313 | HYDROFERA SURGICAL SPEAR | HOZ | 1998-03-02 | 105 |
| K974316 | HYDROFERA FEMORAL WICK | EFQ | 1998-02-13 | 88 |
Recalls
openFDA lists no recalls under a recalling firm named Hydrofera, 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 Hydrofera, LLC?
FDA lists 7 510(k) clearances under the applicant name “Hydrofera, LLC” (first 1998, latest 2019), across 4 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Hydrofera, LLC?
The median time from FDA receipt to decision across 510(k)s cleared under the name Hydrofera, LLC is 119 days.
Which FDA product codes appear under Hydrofera, LLC?
The most frequent FDA product codes under this applicant name are FRO (Dressing, Wound, Drug, 4); EFQ (Gauze/Sponge, Internal, 1); EMX (Balloon, Epistaxis, 1).
Next steps
- See all 7 Hydrofera, LLC clearances with predicates and recalls
- Run predicate analysis for product code FRO, Hydrofera, 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.