Bone Cement, Posterior Screw Augmentation (PML) contract manufacturers

32 US facilities list FDA product code PML as a contract manufacturer (27) or contract sterilizer (5).

FDA-registered (openFDA, export of Oct 21, 2026)

FDA device name

Bone Cement, Posterior Screw Augmentation

Product code

PML (FDA product classification database)

Device class

Class II

Regulation

21 CFR 888.3027

Classification panel

Orthopedic

FDA flags

implant