QGQ
- 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.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K250216 | 2025-09-11 | Active Life Scientific, Inc. | OsteoProbe (OP-100) |
Official FDA classification page: QGQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).