Bryan Corp.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Bryan Corp.” (first 1986, latest 2000), across 5 product codes in 4 review panels. Median 510(k) review time under this name: 127 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 |
|---|---|---|---|
| EOQ | Bronchoscope (Flexible Or Rigid) | 1 | 1 |
| HIF | Insufflator, Laparoscopic | 1 | 1 |
| HIH | Hysteroscope (And Accessories) | 1 | 1 |
| MYU | Accessory, Barium Sulfate, Methyl Methacrylate For Cranioplasty | 1 | 1 |
| NWA | Prosthesis, Tracheal, Preformed/Molded | 1 | 1 |
Review panels
Most recent Bryan Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K002063 | BIOTRACE, MODEL 1730 | MYU | 2000-08-10 | 34 |
| K913242 | MICROPROCESSED CONTROLLED LAPAROFLATOR | HIF | 1992-09-25 | 431 |
| K894380 | DUMON TRACHEOBRONCHIAL STENT | NWA | 1989-10-24 | 99 |
| K881249 | BAGGISH, HYSTEROSCOPE | HIH | 1988-07-28 | 127 |
| K854414 | DUMON/HARRELL | EOQ | 1986-03-12 | 128 |
Recalls
openFDA lists no recalls under a recalling firm named Bryan Corp..
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.
- Bryan Keropian Dds (4 510(k)s)
- Bryan Medical, Inc. (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Bryan Corp.?
FDA lists 5 510(k) clearances under the applicant name “Bryan Corp.” (first 1986, latest 2000), across 5 product codes in 4 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 Bryan Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Bryan Corp. is 127 days.
Which FDA product codes appear under Bryan Corp.?
The most frequent FDA product codes under this applicant name are EOQ (Bronchoscope (Flexible Or Rigid), 1); HIF (Insufflator, Laparoscopic, 1); HIH (Hysteroscope (And Accessories), 1).
Next steps
- See all 5 Bryan Corp. clearances with predicates and recalls
- Run predicate analysis for product code EOQ, Bryan Corp.'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.