QGQ

Bone Indentation Device

Product code
QGQ
Device name
Bone Indentation Device
Device class
Class 2
21 CFR
21 CFR 888.1600
Medical specialty
Orthopedic
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
3 (all years; only the last 3 years are listed here)

FDA classification definition

A bone indentation device is a device that measures resistance to indentation in bone.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2025-09-11.

NumberDecision dateApplicantDevice nameSummary
K2502162025-09-11Active Life Scientific, Inc.OsteoProbe (OP-100)PDF

1 summaries are archived here for direct download.

Official FDA classification page: QGQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).