LOBClass III

Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination

Name: FDA product code LOB: Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination
License: https://open.fda.gov/license/

Unknown

FDA source

LOB is the FDA product code for Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination, a class III device type. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code: LOB
Device name: Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 4

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LOB.