Brimfield Scientific Instruments: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Brimfield Scientific Instruments” (first 1983, latest 1985), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 47 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 |
|---|---|---|---|
| EQH | Source, Carrier, Fiberoptic Light | 1 | 1 |
| FCC | Endoscopic Magnetic Retriever | 1 | 1 |
| GDG | Hook, Surgical, General & Plastic Surgery | 1 | 1 |
| GDZ | Handle, Scalpel | 1 | 1 |
Plus 1 more product codes.
Review panels
Most recent Brimfield Scientific Instruments 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K852042 | BRIMFIELD CANNULATED BLADE HOLDER | GDZ | 1985-06-11 | 33 |
| K843135 | BRIMFIELD CANNULATED MAGNETIC RETRIEVER | FCC | 1984-09-26 | 48 |
| K843136 | BRIMFIELD CANNULATED GRASPING HOOKS | GDG | 1984-09-25 | 47 |
| K841731 | BRIMFIELD FIBEROPTIC LIGHT SCOURCE | EQH | 1984-07-16 | 81 |
| K832147 | CIRCUT 1 | — | 1983-07-26 | 26 |
Recalls
openFDA lists no recalls under a recalling firm named Brimfield Scientific Instruments.
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 Brimfield Scientific Instruments?
FDA lists 5 510(k) clearances under the applicant name “Brimfield Scientific Instruments” (first 1983, latest 1985), across 5 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 Brimfield Scientific Instruments?
The median time from FDA receipt to decision across 510(k)s cleared under the name Brimfield Scientific Instruments is 47 days.
Which FDA product codes appear under Brimfield Scientific Instruments?
The most frequent FDA product codes under this applicant name are EQH (Source, Carrier, Fiberoptic Light, 1); FCC (Endoscopic Magnetic Retriever, 1); GDG (Hook, Surgical, General & Plastic Surgery, 1).
Next steps
- See all 5 Brimfield Scientific Instruments clearances with predicates and recalls
- Run predicate analysis for product code EQH, Brimfield Scientific Instruments'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.