Verite: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Verite” (first 1979, latest 1985), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 68 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 |
|---|---|---|---|
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 6 | 6 |
| IPF | Stimulator, Muscle, Powered | 3 | 3 |
| GZI | Stimulator, Neuromuscular, External Functional | 1 | 1 |
Review panels
- Neurology (7)
- Physical Medicine (3)
Most recent Verite 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K844727 | MODEL 1000 | IPF | 1985-07-09 | 217 |
| K840099 | MODEL 800-A VERI/PPR | GZJ | 1984-11-28 | 323 |
| K840098 | MODEL 811 VERI/TENS & PO | GZJ | 1984-07-17 | 189 |
| K822929 | VERIL/PPR PERSONAL PAIN RELIEVER #800 | GZJ | 1982-11-17 | 44 |
| K820651 | MODEL 860-1 VERI/PROBE | GZJ | 1982-04-29 | 51 |
| K813108 | MODEL 500 VERI/500 | IPF | 1982-02-19 | 108 |
| K813515 | VERI/DFS TM #817 | GZI | 1982-01-19 | 35 |
| K811351 | VERI-FIER | GZJ | 1981-07-30 | 78 |
| K810496 | VERI/PMS MODEL 815 | IPF | 1981-03-13 | 17 |
| K791187 | MODEL 810 VERI/TGS | GZJ | 1979-08-22 | 57 |
Recalls
openFDA lists no recalls under a recalling firm named Verite.
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Verite Scientific, Inc. (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Verite?
FDA lists 10 510(k) clearances under the applicant name “Verite” (first 1979, latest 1985), across 3 product codes in 2 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 Verite?
The median time from FDA receipt to decision across 510(k)s cleared under the name Verite is 68 days.
Which FDA product codes appear under Verite?
The most frequent FDA product codes under this applicant name are GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief, 6); IPF (Stimulator, Muscle, Powered, 3); GZI (Stimulator, Neuromuscular, External Functional, 1).
Next steps
- See all 10 Verite clearances with predicates and recalls
- Run predicate analysis for product code GZJ, Verite'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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.