Data / Medical devices / United States / MPSC

MPSC: FDA-registered device maker in Charlottesville, VA, United States, 1 510(k) clearance

MPSC is registered with the FDA (registration 3007384703) in Charlottesville, VA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 28, 2018. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3007384703

Address

1233 Cedars Court Suite 201, Charlottesville, VA, United States, 22903

Owner or operator

Medical Predictive Science Corporation (10028334)

Roles

Manufacturer

First device listed

January 14, 2020

Registered through

2026

Brand names listed

HeRO Symphony, HeRO ES, HeRO solo/duet

Devices it lists

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.

Compare with other makers

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Updated February 28, 2018. 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.