510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221195Substantially Equivalent

OsteoProbe

Active Life Scientific, Inc., Santa Barbara CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221195 is the FDA 510(k) clearance record for OsteoProbe, a class II device, cleared for Active Life Scientific, Inc. on under FDA product code QGQ (Bone Indentation Device). FDA's definition for product code QGQ reads: "A bone indentation device is a device that measures resistance to indentation in bone". FDA records list 3 510(k) clearances for Active Life Scientific, Inc., from to . As of , FDA records show no recalls naming K221195.

Clearance record

Decision date
Received
(64 days to decision)
Product code
QGQ Bone Indentation Device
Regulation
21 CFR 888.1600
Device class
Class II
Review panel
Orthopedic
Applicant
Active Life Scientific, Inc. 1027 Garden St., Santa Barbara CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QGQ

Trailing 12 months

FDA records hold no clearances under product code QGQ in the trailing twelve months.

FDA records show no clearances under product code QGQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code QGQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260