Bomed Medical Mfr., Ltd.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Bomed Medical Mfr., Ltd.” (first 1981, latest 1986), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 91 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 |
|---|---|---|---|
| DSB | Plethysmograph, Impedance | 4 | 4 |
| DRX | Electrode, Electrocardiograph | 1 | 1 |
| DXG | Computer, Diagnostic, Pre-Programmed, Single-Function | 1 | 1 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 1 | 1 |
| IPF | Stimulator, Muscle, Powered | 1 | 1 |
Review panels
- Cardiovascular (6)
- Neurology (1)
- Physical Medicine (1)
Most recent Bomed Medical Mfr., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K853706 | BOMED-CDM | DSB | 1986-04-14 | 222 |
| K853705 | BOMED-EEA | DRX | 1986-01-13 | 131 |
| K831422 | BIOFLOW | DSB | 1983-09-12 | 132 |
| K831421 | BOMED BIOCON | DSB | 1983-09-12 | 132 |
| K830792 | PULSETTE 110 TRANSCUTANEOUS ELEC-NERVE | GZJ | 1983-03-29 | 15 |
| K813020 | BOMED-NCCOM | DXG | 1981-12-14 | 48 |
| K811999 | BO MED BIA | DSB | 1981-08-31 | 51 |
| K810064 | PULSARII, HIGH VOLT. GALVANIC MUSC. STIM | IPF | 1981-01-26 | 13 |
Recalls
openFDA lists no recalls under a recalling firm named Bomed Medical Mfr., Ltd..
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.
- Bomed Medical Mfg., Ltd. (2 510(k)s)
- Bomed, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Bomed Medical Mfr., Ltd.?
FDA lists 8 510(k) clearances under the applicant name “Bomed Medical Mfr., Ltd.” (first 1981, latest 1986), 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 Bomed Medical Mfr., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Bomed Medical Mfr., Ltd. is 91 days.
Which FDA product codes appear under Bomed Medical Mfr., Ltd.?
The most frequent FDA product codes under this applicant name are DSB (Plethysmograph, Impedance, 4); DRX (Electrode, Electrocardiograph, 1); DXG (Computer, Diagnostic, Pre-Programmed, Single-Function, 1).
Next steps
- See all 8 Bomed Medical Mfr., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code DSB, Bomed Medical Mfr., Ltd.'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.