510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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QGQClass II

Bone Indentation Device

21 CFR 888.1600 / Orthopedic
FDA source (opens on fda.gov)

QGQ is the FDA product code for Bone Indentation Device, a class II device type, regulated under 21 CFR 888.1600. FDA's definition for this code reads: "A bone indentation device is a device that measures resistance to indentation in bone". As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QGQ
Device name
Bone Indentation Device
FDA definition
A bone indentation device is a device that measures resistance to indentation in bone.
Regulation
21 CFR 888.1600
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code QGQ

By decision year
3 clearances under product code QGQ with a decision year between 2021 and 2025, 2021 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QGQ by decision year
YearClearances
20211
20221
20251

Applicants with the most clearances

Product code QGQ
Applicants holding the most 510(k) clearances under product code QGQ
ApplicantClearances
Active Life Scientific, Inc.3

Companies listing this code with FDA

Companies whose registered establishments list this code