fda_clearances_devices
Which companies just cleared or got FDA approval for a medical device? Search openFDA device 510(k) clearances and PMA premarket approvals by applicant company, pathway (510k/pma), FDA product code, advisory-committee specialty (e.g. Cardiovascular), applicant state, or decision date (since). Returns the applicant company (entity-resolved where possible), device name, product code, and decision date — a fresh target list for device and component sellers. openFDA public-domain records. [price: $0.05/row]
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| sort | No | decision_date | date_received :asc|:desc. Default decision_date:desc. | |
| limit | No | Max rows (default 25, cap 100). | |
| since | No | Decision (clearance/approval) date on/after this date (YYYY-MM-DD). | |
| state | No | Applicant state code(s), CSV (510(k) only). | |
| offset | No | Rows to skip. | |
| company | No | Applicant company — suffix/punctuation-insensitive. | |
| pathway | No | 510k | pma (CSV). | |
| entity_id | No | Resolved employer entity UUID. | |
| product_code | No | FDA product code(s), CSV. | |
| advisory_committee | No | Medical specialty panel fragment. |