FDA applicant

Active Optical Systems, Ltd.

Petach-Tikva, IL1 decision2016–20160 recalls

FDA records 1 decision for Active Optical Systems, Ltd. (Petach-Tikva, IL) in 2016: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 1 predicate, 0 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, general and plastic surgery panel, where it files most

How often FDA has decided Active Optical Systems, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Active Optical Systems, Ltd. by year, 2016–2026Sources: 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 Life Scientific, Inc. 3 Active Vertical Correctors, Inc. 2 Active Corp. 1 Active Signal Technologies, Inc. 1 Active Protective Technologies, Inc. 1 Active Optical Systems, Ltd./Efraim Bidas 1

Active Optical Systems, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Active”