Ocean Medical Products, Ltd.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Ocean Medical Products, Ltd.” (first 1981, latest 1988), across 7 product codes in 4 review panels. Median 510(k) review time under this name: 27 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 |
|---|---|---|---|
| GAA | Needle, Aspiration And Injection, Disposable | 3 | 3 |
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | 1 | 1 |
| DRE | Dilator, Vessel, For Percutaneous Catheterization | 1 | 1 |
| DWO | Needle, Biopsy, Cardiovascular | 1 | 1 |
| DYB | Introducer, Catheter | 1 | 1 |
| FMI | Needle, Hypodermic, Single Lumen | 1 | 1 |
| KNW | Instrument, Biopsy | 1 | 1 |
Review panels
Most recent Ocean Medical Products, Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K882013 | SOFT TISSUE BIOPSY DEVICE | DWO | 1988-06-15 | 33 |
| K870896 | NOTCH-NEEDLE, WESCOTT STYLE | GAA | 1987-03-18 | 13 |
| K843719 | SINGLE WALL INTRODUCER NEEDLE | DYB | 1984-10-18 | 24 |
| K823693 | MYELOGRAPHY NEEDLE | FMI | 1983-02-07 | 61 |
| K823692 | SPINAL NEEDLE | BSP | 1983-01-07 | 30 |
| K813462 | MADAYAG TYPE NEEDLE | KNW | 1982-03-01 | 80 |
| K813460 | CHIBA SKINNY NEEDLE | GAA | 1982-01-07 | 27 |
| K813448 | POTTS-COURNAND STYLE NEEDLE | GAA | 1982-01-07 | 27 |
| K813461 | PERCUTANEOUS ENTRY NEEDLE, SELDINGER | DRE | 1981-12-29 | 18 |
Recalls
openFDA lists no recalls under a recalling firm named Ocean Medical Products, 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.
- Ocean Scientific, Inc. (6 510(k)s)
- Ocean Optical Co., Inc. (1 510(k)s)
- Ocean Pacific Med Tec (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Ocean Medical Products, Ltd.?
FDA lists 9 510(k) clearances under the applicant name “Ocean Medical Products, Ltd.” (first 1981, latest 1988), across 7 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 Ocean Medical Products, Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ocean Medical Products, Ltd. is 27 days.
Which FDA product codes appear under Ocean Medical Products, Ltd.?
The most frequent FDA product codes under this applicant name are GAA (Needle, Aspiration And Injection, Disposable, 3); BSP (Needle, Conduction, Anesthetic (W/Wo Introducer), 1); DRE (Dilator, Vessel, For Percutaneous Catheterization, 1).
Next steps
- See all 9 Ocean Medical Products, Ltd. clearances with predicates and recalls
- Run predicate analysis for product code GAA, Ocean Medical Products, 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.