Skip to the page

Data / Medical devices / United States / Ruthless LLC Dba Ruthless Spine

Ruthless LLC Dba Ruthless Spine: FDA-registered device maker in Irwindale, CA, United States, 3 510(k) clearances

Ruthless LLC Dba Ruthless Spine is registered with the FDA (registration 3030150698) in Irwindale, CA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated September 17, 2025. 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
3030150698
Address
1438 Arrow Hwy Ste F, Irwindale, CA, United States, 91706
Owner or operator
Ruthless LLC dba Ruthless Spine (10089525)
Roles
Manufacturer
First device listed
December 14, 2023
Registered through
2026
Brand names listed
Ruthless Spine RJB

Devices it lists

DeviceProduct codeClassRoleSource
Intraoperative Surgical Angle Measurement ToolQWL2Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 17, 2025K252615Ruthless Spine RJBQWLSubstantially EquivalentRuthless, LLC Dba Ruthless Spineaccessdata.fda.gov
November 29, 2024K243375Ruthless Spine RJBQWLSubstantially EquivalentRuthless, LLC Dba Ruthless Spineaccessdata.fda.gov
July 14, 2023DEN230012Ruthless Spine RJBQWLUnknownRuthless, LLC Dba Ruthless Spineaccessdata.fda.gov

Compare with other makers

Updated September 17, 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.