Data / Medical devices / Bone Cement, Posterior Screw Augmentation

Bone Cement, Posterior Screw Augmentation (PML): 65 FDA-registered makers in 9 countries

65 establishments in 9 countries are registered with the FDA to make Bone Cement, Posterior Screw Augmentation (product code PML, Class 2, 21 CFR 888.3027). 26 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 19 510(k) clearances under this code, the latest on June 15, 2026, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code

PML

Device class

2

Regulation

888.3027

Medical specialty

Orthopedic

Implant

Yes

Makers by country

Makers of Bone Cement, Posterior Screw Augmentation

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated June 15, 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.