Data / Medical devices / United States / Proprio
Proprio: FDA-registered device maker in Seattle, WA, United States, 4 510(k) clearances
Proprio is registered with the FDA (registration 3020375573) in Seattle, WA, United States. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated December 15, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3020375573
- Address
- 111 W John St STE 308, Seattle, WA, United States, 98119
- Owner or operator
- Proprio (10087918)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- May 1, 2023
- Registered through
- 2026
- Brand names listed
- Paradigm
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Orthopedic Stereotaxic Instrument | OLO | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 15, 2025 | K252950 | Paradigm System | OLO | Substantially Equivalent | Proprio, Inc. | accessdata.fda.gov |
| June 4, 2025 | K250879 | Paradigm System | OLO | Substantially Equivalent | Proprio, Inc. | accessdata.fda.gov |
| February 21, 2025 | K243258 | Paradigm System | OLO | Substantially Equivalent | Proprio, Inc. | accessdata.fda.gov |
| April 21, 2023 | K222291 | Paradigm System | OLO | Substantially Equivalent | Proprio, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 15, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.