Hyperion, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Hyperion, Inc.” (first 1984, latest 2002), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 78 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 |
|---|---|---|---|
| JJQ | Colorimeter, Photometer, Spectrophotometer For Clinical Use | 4 | 4 |
| DHN | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control | 2 | 2 |
| FPA | Set, Administration, Intravascular | 1 | 1 |
| JQW | Station, Pipetting And Diluting, For Clinical Use | 1 | 1 |
Review panels
- Clinical Chemistry (5)
- Immunology (2)
- General Hospital (1)
Most recent Hyperion, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K022800 | VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM | DHN | 2002-11-25 | 94 |
| K013213 | HYPERION VISIQUANT ANA TEST KIT | DHN | 2002-06-04 | 251 |
| K935983 | MICROREADER 4 | JJQ | 1994-12-09 | 360 |
| K913809 | HY-PREP SYSTEM | JQW | 1992-01-15 | 142 |
| K873138 | MICRO-READER II | JJQ | 1987-09-14 | 35 |
| K864060 | MICRO-READER | JJQ | 1986-11-28 | 39 |
| K855149 | COMPUTING SPECTROPHOTOMETER BIO-CHEMISTRY ANALYZER | JJQ | 1986-02-11 | 47 |
| K834071 | LYMPHANGIOGRAPHY SET SPECIAL 30G | FPA | 1984-01-25 | 61 |
Recalls
openFDA lists no recalls under a recalling firm named Hyperion, 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 Hyperion, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Hyperion, Inc.” (first 1984, latest 2002), 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 Hyperion, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Hyperion, Inc. is 78 days.
Which FDA product codes appear under Hyperion, Inc.?
The most frequent FDA product codes under this applicant name are JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use, 4); DHN (Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control, 2); FPA (Set, Administration, Intravascular, 1).
Next steps
- See all 8 Hyperion, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JJQ, Hyperion, 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.