Marizyme: FDA filings under this applicant name
FDA lists 1 510(k) clearance under the applicant name “Marizyme” (first 2024, latest 2024), plus 1 De Novo decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 27 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 |
|---|---|---|
| 2024 | 1 | 27 |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Marizyme took a median 27 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 27 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| QEJ | Flushing Solution For Short Term Storage Of Veins At Room Temperature During Coronary Artery Bypass Graft Surgeries | 2 | 1 |
Review panels
Most recent Marizyme 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K240925 | DuraGraft Vascular Conduit Solution | QEJ | 2024-05-01 | 27 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| DEN230002 | De Novo | Flushing Solution For Short Term Storage Of Veins At Room Temperature During Coronary Artery Bypass Graft Surgeries | 2023-10-04 |
Recalls
openFDA lists no recalls under a recalling firm named Marizyme.
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 Marizyme?
FDA lists 1 510(k) clearance under the applicant name “Marizyme” (first 2024, latest 2024), plus 1 De Novo decision, across 1 product code 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 Marizyme?
The median time from FDA receipt to decision across 510(k)s cleared under the name Marizyme is 27 days.
Which FDA product codes appear under Marizyme?
The most frequent FDA product codes under this applicant name are QEJ (Flushing Solution For Short Term Storage Of Veins At Room Temperature During Coronary Artery Bypass Graft Surgeries, 2).
Next steps
- See all 1 Marizyme clearances with predicates and recalls
- Run predicate analysis for product code QEJ, Marizyme'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.