Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Thoracic / United States

FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Thoracic in the United States: 66 establishments

66 establishments in the United States are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Thoracic (product code PHM). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device

Intervertebral Fusion Device With Bone Graft, Thoracic

Product code

PHM

Country

United States

Makers of Intervertebral Fusion Device With Bone Graft, Thoracic in the United States

Updated November 2, 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.