Biosonics, Inc.: FDA filings under this applicant name
FDA lists 3 510(k) clearances under the applicant name “Biosonics, Inc.” (first 1986, latest 1988), plus 1 PMA decision, across 2 product codes in 2 review panels. Median 510(k) review time under this name: 86 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 |
|---|---|---|---|
| KPN | Alarm, Conditioned Response Enuresis | 3 | 3 |
| LTF | Stimulator, Salivary System | 1 | 0 |
Review panels
Most recent Biosonics, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K882555 | ANOTRON(R) INCONTINENCE CONTROL SYSTEM | KPN | 1988-08-30 | 70 |
| K864448 | THE BIOSONICS CONTINENCE CONTROL SYSTEM CCS(TM) | KPN | 1987-02-06 | 86 |
| K862683 | BIOSOICS SPHINCTER TRAINING SYSTEM | KPN | 1986-11-12 | 120 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P860067 | PMA | SALITRON SYSTEM | 1988-05-17 |
Recalls
openFDA lists no recalls under a recalling firm named Biosonics, 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 Biosonics, Inc.?
FDA lists 3 510(k) clearances under the applicant name “Biosonics, Inc.” (first 1986, latest 1988), plus 1 PMA decision, across 2 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 Biosonics, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Biosonics, Inc. is 86 days.
Which FDA product codes appear under Biosonics, Inc.?
The most frequent FDA product codes under this applicant name are KPN (Alarm, Conditioned Response Enuresis, 3); LTF (Stimulator, Salivary System, 1).
Next steps
- See all 3 Biosonics, Inc. clearances with predicates and recalls
- Run predicate analysis for product code KPN, Biosonics, 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.