Beam-Med, Ltd.: FDA filings under this applicant name
FDA lists 1 510(k) clearance under the applicant name “Beam-Med, Ltd.” (first 2011, latest 2011), plus 1 PMA decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 222 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 |
|---|---|---|---|
| MUA | Bone Sonometer | 2 | 1 |
Review panels
- Radiology (2)
Most recent Beam-Med, Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K110646 | BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER | MUA | 2011-10-12 | 222 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P990035 | PMA | THE SUNLIGHT OMNISENSE(TM) ULTRASOUND BONE SONOMETER | 2000-01-20 |
Recalls
openFDA lists no recalls under a recalling firm named Beam-Med, 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.
- Beam Tech , Ltd. (1 510(k)s)
- Beam Technologies, LLC (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Beam-Med, Ltd.?
FDA lists 1 510(k) clearance under the applicant name “Beam-Med, Ltd.” (first 2011, latest 2011), plus 1 PMA decision, 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 Beam-Med, Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Beam-Med, Ltd. is 222 days.
Which FDA product codes appear under Beam-Med, Ltd.?
The most frequent FDA product codes under this applicant name are MUA (Bone Sonometer, 2).
Next steps
- See all 1 Beam-Med, Ltd. clearances with predicates and recalls
- Run predicate analysis for product code MUA, Beam-Med, 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 (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.