FDA applicant

Active Life Scientific, Inc.

Santa Barbara, CA3 decisions2021–20250 recalls

FDA records 3 decisions for Active Life Scientific, Inc. (Santa Barbara, CA) from 2021 to 2025: 2 510(k) clearances and 1 De Novo grant. All are in product code QGQ (Bone Indentation Device). Its devices cite 2 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Active Life Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2021high 1 (2021) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Active Life Scientific, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Active”

FDA records each applicant name separately; these may or may not be the same firm.

Active Electronics, Inc. 7 Active Vertical Correctors, Inc. 2 Active Corp. 1 Active Optical Systems, Ltd. 1 Active Signal Technologies, Inc. 1 Active Protective Technologies, Inc. 1 Active Optical Systems, Ltd./Efraim Bidas 1

Active Life Scientific, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Active”