Vxr, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Vxr, Inc.” (first 1983, latest 1985), across 7 product codes in 3 review panels. Median 510(k) review time under this name: 52 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 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| JHI | Visual, Pregnancy Hcg, Prescription Use | 2 | 2 |
| CDP | Radioimmunoassay, Total Triiodothyronine | 1 | 1 |
| ETD | Tube, Tympanostomy | 1 | 1 |
| JIX | Calibrator, Multi-Analyte Mixture | 1 | 1 |
| KLI | Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine | 1 | 1 |
| KLS | Enzyme Immunoassay, Theophylline | 1 | 1 |
| KXT | Enzyme Immunoassay, Digoxin | 1 | 1 |
Review panels
Most recent Vxr, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K853703 | VENTREZYME T3 IMMUNOASSAY T3 | CDP | 1985-10-04 | 30 |
| K853748 | VENTRESCREEN HCG URINE | JHI | 1985-10-01 | 22 |
| K841456 | VENTREXYME EIA CONTROLS IMMUNOASSAY | JIX | 1984-05-21 | 42 |
| K840473 | VENTREZYME T4 IMMUNOASSAY T4 | KLI | 1984-04-04 | 61 |
| K833960 | VENTREX PREGNANCY TEST KIT ENZYME | JHI | 1984-02-03 | 79 |
| K833989 | VENTREZYME THEOPHYLLINE IMMUNOASSAY | KLS | 1984-01-30 | 73 |
| K833878 | VENTREZYME DIGOXIN IMMUNOASSAY DIGOX | KXT | 1984-01-13 | 66 |
| K833909 | VENTRESCREEN BETA-HCG ENZYME IMMUNO | ETD | 1983-11-21 | 7 |
Recalls
openFDA lists no recalls under a recalling firm named Vxr, 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 Vxr, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Vxr, Inc.” (first 1983, latest 1985), across 7 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 Vxr, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Vxr, Inc. is 52 days.
Which FDA product codes appear under Vxr, Inc.?
The most frequent FDA product codes under this applicant name are JHI (Visual, Pregnancy Hcg, Prescription Use, 2); CDP (Radioimmunoassay, Total Triiodothyronine, 1); ETD (Tube, Tympanostomy, 1).
Next steps
- See all 8 Vxr, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JHI, Vxr, 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.