Moe: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Moe” (first 1989, latest 1989), across 1 product code in 1 review panel. Median 510(k) review time under this name: 76 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 |
|---|---|---|---|
| HCC | Device, Biofeedback | 6 | 6 |
Review panels
- Neurology (6)
Most recent Moe 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K884849 | BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR | HCC | 1989-03-23 | 125 |
| K884851 | BIOFEEDBACK DEVICE TG3, TG4 | HCC | 1989-02-03 | 77 |
| K884853 | BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1 | HCC | 1989-02-02 | 76 |
| K884852 | BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI. | HCC | 1989-02-02 | 76 |
| K884850 | BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 | HCC | 1989-02-02 | 76 |
| K884848 | BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV | HCC | 1989-02-02 | 76 |
Recalls
openFDA lists no recalls under a recalling firm named Moe.
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 Moe?
FDA lists 6 510(k) clearances under the applicant name “Moe” (first 1989, latest 1989), 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 Moe?
The median time from FDA receipt to decision across 510(k)s cleared under the name Moe is 76 days.
Which FDA product codes appear under Moe?
The most frequent FDA product codes under this applicant name are HCC (Device, Biofeedback, 6).
Next steps
- See all 6 Moe clearances with predicates and recalls
- Run predicate analysis for product code HCC, Moe'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.