Data / Medical devices / United States / Linear Health Sciences LLC

Linear Health Sciences LLC: FDA-registered device maker in Norman, OK, United States, 4 510(k) clearances

Linear Health Sciences LLC is registered with the FDA (registration 3017705285) in Norman, OK, United States. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated September 6, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number

3017705285

Address

1125 N Porter Ave Ste 205, Norman, OK, United States, 73071

Owner or operator

Linear Health Sciences LLC (10085487)

Roles

Specification developer

First device listed

June 23, 2022

Registered through

2026

Brand names listed

Orchid Safety Release Valve

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 Intravenous Catheter Force-Activated Separation Device.

Updated September 6, 2024. 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.