Data / Medical devices / United States / Modular Medical

Modular Medical: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance

Modular Medical is registered with the FDA (registration 3027453514) in San Diego, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 8, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number

3027453514

Address

10740 Thornmint Rd, San Diego, CA, United States, 92127

Owner or operator

Modular Medical (10092199)

Roles

Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer

First device listed

May 7, 2026

Registered through

2026

Brand names listed

Pivot Insulin Delivery System

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

• All makers of Pump, Infusion, Insulin

Updated April 8, 2026. 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.